Terry Hassold - Publications

Genetics and Cell Biology Washington State University, Pullman, WA, United States 

180 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Hassold TJ, Hunt PA. Missed connections: Recombination and human aneuploidy. Prenatal Diagnosis. PMID 33484483 DOI: 10.1002/pd.5910  0.32
2020 Hassold T, Maylor-Hagen H, Wood A, Gruhn J, Hoffmann E, Broman KW, Hunt P. Failure to recombine is a common feature of human oogenesis. American Journal of Human Genetics. PMID 33306948 DOI: 10.1016/j.ajhg.2020.11.010  0.32
2017 Horan TS, Marre A, Hassold T, Lawson C, Hunt PA. Correction: Germline and reproductive tract effects intensify in male mice with successive generations of estrogenic exposure. Plos Genetics. 13: e1006980. PMID 28854188 DOI: 10.1371/journal.pgen.1006980  0.32
2017 Horan TS, Marre A, Hassold T, Lawson C, Hunt PA. Germline and reproductive tract effects intensify in male mice with successive generations of estrogenic exposure. Plos Genetics. 13: e1006885. PMID 28727826 DOI: 10.1371/Journal.Pgen.1006885  0.32
2016 Hardy K, Hardy PJ, Jacobs PA, Lewallen K, Hassold TJ. Temporal changes in chromosome abnormalities in human spontaneous abortions: Results of 40 years of analysis. American Journal of Medical Genetics. Part A. PMID 27287007 DOI: 10.1002/ajmg.a.37795  0.32
2016 Gruhn JR, Al-Asmar N, Fasnacht R, Maylor-Hagen H, Peinado V, Rubio C, Broman KW, Hunt PA, Hassold T. Correlations between Synaptic Initiation and Meiotic Recombination: A Study of Humans and Mice. American Journal of Human Genetics. 98: 102-15. PMID 26749305 DOI: 10.1016/J.Ajhg.2015.11.019  0.32
2015 Vrooman LA, Oatley JM, Griswold JE, Hassold TJ, Hunt PA. Estrogenic exposure alters the spermatogonial stem cells in the developing testis, permanently reducing crossover levels in the adult. Plos Genetics. 11: e1004949. PMID 25615633 DOI: 10.1371/Journal.Pgen.1004949  0.32
2014 Rowsey R, Gruhn J, Broman KW, Hunt PA, Hassold T. Examining variation in recombination levels in the human female: a test of the production-line hypothesis. American Journal of Human Genetics. 95: 108-12. PMID 24995869 DOI: 10.1097/Ogx.0000000000000135  0.32
2014 Baier B, Hunt P, Broman KW, Hassold T. Variation in genome-wide levels of meiotic recombination is established at the onset of prophase in mammalian males. Plos Genetics. 10: e1004125. PMID 24497841 DOI: 10.1371/Journal.Pgen.1004125  0.32
2014 Vrooman LA, Nagaoka SI, Hassold TJ, Hunt PA. Evidence for paternal age-related alterations in meiotic chromosome dynamics in the mouse. Genetics. 196: 385-96. PMID 24318536 DOI: 10.1534/Genetics.113.158782  0.32
2013 Gruhn JR, Rubio C, Broman KW, Hunt PA, Hassold T. Cytological studies of human meiosis: sex-specific differences in recombination originate at, or prior to, establishment of double-strand breaks. Plos One. 8: e85075. PMID 24376867 DOI: 10.1371/Journal.Pone.0085075  0.32
2013 Rowsey R, Kashevarova A, Murdoch B, Dickenson C, Woodruff T, Cheng E, Hunt P, Hassold T. Germline mosaicism does not explain the maternal age effect on trisomy. American Journal of Medical Genetics. Part A. 161: 2495-503. PMID 23950106 DOI: 10.1002/Ajmg.A.36120  0.32
2013 Murdoch B, Owen N, Stevense M, Smith H, Nagaoka S, Hassold T, McKay M, Xu H, Fu J, Revenkova E, Jessberger R, Hunt P. Altered cohesin gene dosage affects Mammalian meiotic chromosome structure and behavior. Plos Genetics. 9: e1003241. PMID 23408896 DOI: 10.1371/Journal.Pgen.1003241  0.32
2013 Johnson ME, Rowsey RA, Shirley S, Vandevoort C, Bailey J, Hassold T. A specific family of interspersed repeats (SINEs) facilitates meiotic synapsis in mammals. Molecular Cytogenetics. 6: 1. PMID 23276256 DOI: 10.1186/1755-8166-6-1  0.32
2012 Hunt PA, Lawson C, Gieske M, Murdoch B, Smith H, Marre A, Hassold T, VandeVoort CA. Bisphenol A alters early oogenesis and follicle formation in the fetal ovary of the rhesus monkey. Proceedings of the National Academy of Sciences of the United States of America. 109: 17525-30. PMID 23012422 DOI: 10.1073/Pnas.1207854109  0.32
2012 Nagaoka SI, Hassold TJ, Hunt PA. Human aneuploidy: mechanisms and new insights into an age-old problem. Nature Reviews. Genetics. 13: 493-504. PMID 22705668 DOI: 10.1038/nrg3245  0.32
2012 Al-Asmar N, Peinado V, Vera M, Remohí J, Pellicer A, Simón C, Hassold T, Rubio C. Chromosomal abnormalities in embryos from couples with a previous aneuploid miscarriage. Fertility and Sterility. 98: 145-50. PMID 22521156 DOI: 10.1016/J.Fertnstert.2012.03.035  0.32
2011 Gabriel AS, Hassold TJ, Thornhill AR, Affara NA, Handyside AH, Griffin DK. An algorithm for determining the origin of trisomy and the positions of chiasmata from SNP genotype data. Chromosome Research : An International Journal On the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology. 19: 155-63. PMID 21225334 DOI: 10.1007/s10577-010-9181-4  0.32
2011 Lawson C, Gieske M, Murdoch B, Ye P, Li Y, Hassold T, Hunt PA. Gene expression in the fetal mouse ovary is altered by exposure to low doses of bisphenol A. Biology of Reproduction. 84: 79-86. PMID 20739668 DOI: 10.1095/Biolreprod.110.084814  0.32
2011 Gruhn JR, Broman KW, Hunt PA, Hassold TJ. The embryo/blastomere: Meiotic recombination in human oocytes Stem Cells in Reproductive Medicine: Basic Science and Therapeutic Potential. 63-75. DOI: 10.1017/CBO9781139540742.007  0.32
2010 Billings T, Sargent EE, Szatkiewicz JP, Leahy N, Kwak IY, Bektassova N, Walker M, Hassold T, Graber JH, Broman KW, Petkov PM. Patterns of recombination activity on mouse chromosome 11 revealed by high resolution mapping. Plos One. 5: e15340. PMID 21170346 DOI: 10.1371/Journal.Pone.0015340  0.32
2010 Murdoch B, Owen N, Shirley S, Crumb S, Broman KW, Hassold T. Multiple loci contribute to genome-wide recombination levels in male mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 550-5. PMID 21113599 DOI: 10.1007/S00335-010-9303-5  0.32
2010 Hunt P, Hassold T. Female meiosis: coming unglued with age. Current Biology : Cb. 20: R699-702. PMID 20833308 DOI: 10.1016/J.Cub.2010.08.011  0.32
2010 Zheng P, Griswold MD, Hassold TJ, Hunt PA, Small CL, Ye P. Predicting meiotic pathways in human fetal oogenesis. Biology of Reproduction. 82: 543-51. PMID 19846598 DOI: 10.1095/Biolreprod.109.079590  0.32
2010 Keats BJB, Hassold TJ. Recollections from 60 ASHG meetings American Journal of Human Genetics. 87: 580-592. DOI: 10.1016/j.ajhg.2010.10.011  0.32
2009 Hassold T, Hunt P. Maternal age and chromosomally abnormal pregnancies: what we know and what we wish we knew. Current Opinion in Pediatrics. 21: 703-8. PMID 19881348 DOI: 10.1097/MOP.0b013e328332c6ab  0.32
2009 Cheng EY, Hunt PA, Naluai-Cecchini TA, Fligner CL, Fujimoto VY, Pasternack TL, Schwartz JM, Steinauer JE, Woodruff TJ, Cherry SM, Hansen TA, Vallente RU, Broman KW, Hassold TJ. Meiotic recombination in human oocytes. Plos Genetics. 5: e1000661. PMID 19763179 DOI: 10.1371/Journal.Pgen.1000661  0.32
2009 Hunt PA, Susiarjo M, Rubio C, Hassold TJ. The bisphenol A experience: a primer for the analysis of environmental effects on mammalian reproduction. Biology of Reproduction. 81: 807-13. PMID 19458313 DOI: 10.1095/biolreprod.109.077008  0.32
2009 Hassold T, Hansen T, Hunt P, Vandevoort C. Cytological studies of recombination in rhesus males Cytogenetic and Genome Research. 124: 132-138. PMID 19420925 DOI: 10.1159/000207519  0.32
2009 Houmard B, Small C, Yang L, Naluai-Cecchini T, Cheng E, Hassold T, Griswold M. Global gene expression in the human fetal testis and ovary. Biology of Reproduction. 81: 438-43. PMID 19369649 DOI: 10.1095/Biolreprod.108.075747  0.32
2009 Myers JP, vom Saal FS, Akingbemi BT, Arizono K, Belcher S, Colborn T, Chahoud I, Crain DA, Farabollini F, Guillette LJ, Hassold T, Ho SM, Hunt PA, Iguchi T, Jobling S, et al. Why public health agencies cannot depend on good laboratory practices as a criterion for selecting data: the case of bisphenol A. Environmental Health Perspectives. 117: 309-15. PMID 19337501 DOI: 10.1289/Ehp.0800173  0.32
2009 Muhlhauser A, Susiarjo M, Rubio C, Griswold J, Gorence G, Hassold T, Hunt PA. Bisphenol A effects on the growing mouse oocyte are influenced by diet. Biology of Reproduction. 80: 1066-71. PMID 19164168 DOI: 10.1095/Biolreprod.108.074815  0.32
2009 Hunt PA, Hassold T. BPA: traditional toxicology testing is inadequate and concerns extend beyond aneuploidy Trends in Genetics. 25: 15-16. DOI: 10.1016/J.Tig.2008.10.006  0.32
2008 Anderson EL, Baltus AE, Roepers-Gajadien HL, Hassold TJ, de Rooij DG, van Pelt AM, Page DC. Stra8 and its inducer, retinoic acid, regulate meiotic initiation in both spermatogenesis and oogenesis in mice. Proceedings of the National Academy of Sciences of the United States of America. 105: 14976-80. PMID 18799751 DOI: 10.1073/Pnas.0807297105  0.32
2008 Sanderson ML, Hassold TJ, Carrell DT. Proteins involved in meiotic recombination: a role in male infertility? Systems Biology in Reproductive Medicine. 54: 57-74. PMID 18446647 DOI: 10.1080/19396360701881922  0.32
2008 Hunt PA, Hassold TJ. Human female meiosis: what makes a good egg go bad? Trends in Genetics : Tig. 24: 86-93. PMID 18192063 DOI: 10.1016/j.tig.2007.11.010  0.32
2007 Hassold T, Hall H, Hunt P. The origin of human aneuploidy: where we have been, where we are going. Human Molecular Genetics. 16: R203-8. PMID 17911163 DOI: 10.1093/Hmg/Ddm243  0.32
2007 Hassold T, Hunt P. Rescuing distal crossovers. Nature Genetics. 39: 1187-8. PMID 17898774 DOI: 10.1038/Ng1007-1187  0.32
2007 Hall HE, Chan ER, Collins A, Judis L, Shirley S, Surti U, Hoffner L, Cockwell AE, Jacobs PA, Hassold TJ. The origin of trisomy 13. American Journal of Medical Genetics. Part A. 143: 2242-8. PMID 17853475 DOI: 10.1002/Ajmg.A.31913  0.32
2007 Hall HE, Surti U, Hoffner L, Shirley S, Feingold E, Hassold T. The origin of trisomy 22: evidence for acrocentric chromosome-specific patterns of nondisjunction. American Journal of Medical Genetics. Part A. 143: 2249-55. PMID 17705154 DOI: 10.1002/Ajmg.A.31918  0.32
2007 Cherry SM, Adelman CA, Theunissen JW, Hassold TJ, Hunt PA, Petrini JH. The Mre11 complex influences DNA repair, synapsis, and crossing over in murine meiosis. Current Biology : Cb. 17: 373-8. PMID 17291760 DOI: 10.1016/J.Cub.2006.12.048  0.32
2007 Susiarjo M, Hassold TJ, Freeman E, Hunt PA. Bisphenol A exposure in utero disrupts early oogenesis in the mouse. Plos Genetics. 3: e5. PMID 17222059 DOI: 10.1371/journal.pgen.0030005  0.32
2007 Topping D, Brown P, Hassold T. The immunocytogenetics of human male meiosis: A progress report The Genetics of Male Infertility. 115-128. DOI: 10.1007/978-1-59745-176-5_7  0.32
2006 Koehler KE, Schrump SE, Cherry JP, Hassold TJ, Hunt PA. Near-human aneuploidy levels in female mice with homeologous chromosomes. Current Biology : Cb. 16: R579-80. PMID 16890511 DOI: 10.1016/j.cub.2006.07.018  0.32
2006 Topping D, Brown P, Judis L, Schwartz S, Seftel A, Thomas A, Hassold T. Synaptic defects at meiosis I and non-obstructive azoospermia. Human Reproduction (Oxford, England). 21: 3171-7. PMID 16861745 DOI: 10.1093/Humrep/Del281  0.32
2006 Hall H, Hunt P, Hassold T. Meiosis and sex chromosome aneuploidy: how meiotic errors cause aneuploidy; how aneuploidy causes meiotic errors. Current Opinion in Genetics & Development. 16: 323-9. PMID 16647844 DOI: 10.1016/J.Gde.2006.04.011  0.32
2006 Vallente RU, Cheng EY, Hassold TJ. The synaptonemal complex and meiotic recombination in humans: new approaches to old questions. Chromosoma. 115: 241-9. PMID 16547726 DOI: 10.1007/s00412-006-0058-4  0.32
2005 Hodges CA, Revenkova E, Jessberger R, Hassold TJ, Hunt PA. SMC1beta-deficient female mice provide evidence that cohesins are a missing link in age-related nondisjunction. Nature Genetics. 37: 1351-5. PMID 16258540 DOI: 10.1038/ng1672  0.32
2005 Lamb NE, Sherman SL, Hassold TJ. Effect of meiotic recombination on the production of aneuploid gametes in humans Cytogenetic and Genome Research. 111: 250-255. PMID 16192701 DOI: 10.1159/000086896  0.32
2005 Lynn A, Schrump S, Cherry J, Hassold T, Hunt P. Sex, not genotype, determines recombination levels in mice. American Journal of Human Genetics. 77: 670-5. PMID 16175513 DOI: 10.1086/491718  0.32
2005 Brown PW, Judis L, Chan ER, Schwartz S, Seftel A, Thomas A, Hassold TJ. Meiotic synapsis proceeds from a limited number of subtelomeric sites in the human male. American Journal of Human Genetics. 77: 556-66. PMID 16175502 DOI: 10.1086/468188  0.32
2005 Mann MB, Hodges CA, Barnes E, Vogel H, Hassold TJ, Luo G. Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome. Human Molecular Genetics. 14: 813-25. PMID 15703196 DOI: 10.1093/Hmg/Ddi075  0.32
2004 Lamb NE, Hassold TJ. Nondisjunction--a view from ringside. The New England Journal of Medicine. 351: 1931-4. PMID 15525719 DOI: 10.1056/NEJMp048118  0.32
2004 Cherry SM, Hunt PA, Hassold TJ. Cisplatin disrupts mammalian spermatogenesis, but does not affect recombination or chromosome segregation. Mutation Research. 564: 115-28. PMID 15507376 DOI: 10.1016/j.mrgentox.2004.08.010  0.32
2004 Lynn A, Ashley T, Hassold T. Variation in human meiotic recombination. Annual Review of Genomics and Human Genetics. 5: 317-49. PMID 15485352 DOI: 10.1146/Annurev.Genom.4.070802.110217  0.32
2004 Hassold T, Judis L, Chan ER, Schwartz S, Seftel A, Lynn A. Cytological studies of meiotic recombination in human males Cytogenetic and Genome Research. 107: 249-255. PMID 15467369 DOI: 10.1159/000080602  0.32
2004 Koehler KE, Millie EA, Cherry JP, Schrump SE, Hassold TJ. Meiotic exchange and segregation in female mice heterozygous for paracentric inversions. Genetics. 166: 1199-214. PMID 15082541 DOI: 10.1534/genetics.166.3.1199  0.32
2004 Judis L, Chan ER, Schwartz S, Seftel A, Hassold T. Meiosis I arrest and azoospermia in an infertile male explained by failure of formation of a component of the synaptonemal complex. Fertility and Sterility. 81: 205-9. PMID 14711569 DOI: 10.1016/J.Fertnstert.2003.05.021  0.32
2004 Hassold T, Pettay D, May K, Robinson A. Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy Human Genetics. 85: 648-650. PMID 1977687 DOI: 10.1007/Bf00193591  0.32
2004 Hassold T, Pettay D, Robinson A, Uchida I. Molecular studies of parental origin and mosaicism in 45,X conceptuses Human Genetics. 89: 647-652. PMID 1511983 DOI: 10.1007/Bf00221956  0.32
2003 Koehler KE, Voigt RC, Thomas S, Lamb B, Urban C, Hassold T, Hunt PA. When disaster strikes: rethinking caging materials. Lab Animal. 32: 24-7. PMID 19753748 DOI: 10.1038/Laban0403-24  0.32
2003 Simpson JL, de la Cruz F, Swerdloff RS, Samango-Sprouse C, Skakkebaek NE, Graham JM, Hassold T, Aylstock M, Meyer-Bahlburg HF, Willard HF, Hall JG, Salameh W, Boone K, Staessen C, Geschwind D, et al. Klinefelter syndrome: expanding the phenotype and identifying new research directions. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 5: 460-8. PMID 14614399 DOI: 10.1097/01.Gim.0000095626.54201.D0  0.32
2003 Thomas NS, Hassold TJ. Aberrant recombination and the origin of Klinefelter syndrome Human Reproduction Update. 9: 309-317. PMID 12926525 DOI: 10.1093/humupd/dmg028  0.32
2003 Hunt PA, Koehler KE, Susiarjo M, Hodges CA, Ilagan A, Voigt RC, Thomas S, Thomas BF, Hassold TJ. Bisphenol a exposure causes meiotic aneuploidy in the female mouse. Current Biology : Cb. 13: 546-53. PMID 12676084 DOI: 10.1016/S0960-9822(03)00189-1  0.32
2002 Koehler KE, Millie EA, Cherry JP, Burgoyne PS, Evans EP, Hunt PA, Hassold TJ. Sex-specific differences in meiotic chromosome segregation revealed by dicentric bridge resolution in mice. Genetics. 162: 1367-79. PMID 12454080  0.32
2002 Koehler KE, Cherry JP, Lynn A, Hunt PA, Hassold TJ. Genetic control of mammalian meiotic recombination. I. Variation in exchange frequencies among males from inbred mouse strains. Genetics. 162: 297-306. PMID 12242241  0.32
2002 Bean CJ, Hassold TJ, Judis L, Hunt PA. Fertilization in vitro increases non-disjunction during early cleavage divisions in a mouse model system. Human Reproduction (Oxford, England). 17: 2362-7. PMID 12202426  0.32
2002 Hunt PA, Hassold TJ. Sex matters in meiosis. Science (New York, N.Y.). 296: 2181-3. PMID 12077403 DOI: 10.1126/science.1071907  0.32
2002 Lynn A, Koehler KE, Judis L, Chan ER, Cherry JP, Schwartz S, Seftel A, Hunt PA, Hassold TJ. Covariation of synaptonemal complex length and mammalian meiotic exchange rates. Science (New York, N.Y.). 296: 2222-5. PMID 12052900 DOI: 10.1126/science.1071220  0.32
2001 Hassold TJ, Burrage LC, Chan ER, Judis LM, Schwartz S, James SJ, Jacobs PA, Thomas NS. Maternal folate polymorphisms and the etiology of human nondisjunction. American Journal of Human Genetics. 69: 434-9. PMID 11443546 DOI: 10.1086/321971  0.32
2001 Bean CJ, Hunt PA, Millie EA, Hassold TJ. Analysis of a malsegregating mouse Y chromosome: evidence that the earliest cleavage divisions of the mammalian embryo are non-disjunction-prone. Human Molecular Genetics. 10: 963-72. PMID 11309370  0.32
2001 Hassold T, Hunt P. To err (meiotically) is human: The genesis of human aneuploidy Nature Reviews Genetics. 2: 280-291. PMID 11283700 DOI: 10.1038/35066065  0.32
2001 Thomas NS, Ennis S, Sharp AJ, Durkie M, Hassold TJ, Collins AR, Jacobs PA. Maternal sex chromosome non-disjunction: Evidence for X chromosome-specific risk factors Human Molecular Genetics. 10: 243-250. PMID 11159943  0.32
2000 Thomas NS, Collins AR, Hassold TJ, Jacobs PA. A reinvestigation of non-disjunction resulting in 47, XXY males of paternal origin. European Journal of Human Genetics : Ejhg. 8: 805-8. PMID 11039584 DOI: 10.1038/sj.ejhg.5200531  0.32
2000 Hixon ML, Muro-Cacho C, Wagner MW, Obejero-Paz C, Millie E, Fujio Y, Kureishi Y, Hassold T, Walsh K, Gualberto A. Akt1/PKB upregulation leads to vascular smooth muscle cell hypertrophy and polyploidization. The Journal of Clinical Investigation. 106: 1011-20. PMID 11032861 DOI: 10.1172/Jci8252  0.32
2000 Hixon ML, Obejero-Paz C, Muro-Cacho C, Wagner MW, Millie E, Nagy J, Hassold TJ, Gualberto A. Cks1 mediates vascular smooth muscle cell polyploidization. The Journal of Biological Chemistry. 275: 40434-42. PMID 11005810 DOI: 10.1074/Jbc.M005059200  0.32
2000 Hassold T, Sherman S, Hunt P. Counting cross-overs: Characterizing meiotic recombination in mammals Human Molecular Genetics. 9: 2409-2419. PMID 11005796 DOI: 10.1093/Hmg/9.16.2409  0.32
2000 LePage DF, Church DM, Millie E, Hassold TJ, Conlon RA. Rapid generation of nested chromosomal deletions on mouse chromosome 2. Proceedings of the National Academy of Sciences of the United States of America. 97: 10471-6. PMID 10984539 DOI: 10.1073/Pnas.97.19.10471  0.32
2000 Robinson WP, Christian SL, Kuchinka BD, Peñaherrera MS, Das S, Schuffenhauer S, Malcolm S, Schinzel AA, Hassold TJ, Ledbetter DH. Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15 Clinical Genetics. 57: 349-358. PMID 10852369 DOI: 10.1034/J.1399-0004.2000.570505.X  0.32
2000 Zaragoza MV, Surti U, Redline RW, Millie E, Chakravarti A, Hassold TJ. Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole. American Journal of Human Genetics. 66: 1807-20. PMID 10801385 DOI: 10.1086/302951  0.32
2000 Hassold T, Sherman S. Down syndrome: Genetic recombination and the origin of the extra chromosome 21 Clinical Genetics. 57: 95-100. PMID 10735628 DOI: 10.1034/J.1399-0004.2000.570201.X  0.32
1999 Shield JP, Wadsworth EJ, Hassold TJ, Judis LA, Jacobs PA. Is disomic homozygosity at the APECED locus the cause of increased autoimmunity in Down's syndrome? Archives of Disease in Childhood. 81: 147-50. PMID 10490523  0.32
1999 Padungtod C, Hassold TJ, Millie E, Ryan LM, Savitz DA, Christiani DC, Xu X. Sperm aneuploidy among Chinese pesticide factory workers: scoring by the FISH method. American Journal of Industrial Medicine. 36: 230-8. PMID 10398931 DOI: 10.1002/(Sici)1097-0274(199908)36:2<230::Aid-Ajim2>3.0.Co;2-6  0.32
1999 Mroz K, Hassold TJ, Hunt PA. Meiotic aneuploidy in the XXY mouse: Evidence that a compromised testicular environment increases the incidence of meiotic errors Human Reproduction. 14: 1151-1156. PMID 10325252 DOI: 10.1093/humrep/14.5.1151  0.32
1999 Redline RW, Zaragoza M, Hassold T. Prevalence of developmental and inflammatory lesions in nonmolar first- trimester spontaneous abortions Human Pathology. 30: 93-100. PMID 9923934 DOI: 10.1016/S0046-8177(99)90307-6  0.32
1998 Koehler KE, Hassold TJ. Human aneuploidy: Lessons from achiasmate segregation in Drosophila melanogaster Annals of Human Genetics. 62: 467-479. PMID 10363125 DOI: 10.1017/S0003480098007179  0.32
1998 Hixon M, Millie E, Judis LA, Sherman S, Allran K, Taft L, Hassold T. FISH studies of the sperm of fathers of paternally derived cases of trisomy 21: no evidence for an increase in aneuploidy. Human Genetics. 103: 654-7. PMID 9921898 DOI: 10.1007/S004390050886  0.32
1998 Freeman SB, Taft LF, Dooley KJ, Allran K, Sherman SL, Hassold TJ, Khoury MJ, Saker DM. Population-based study of congenital heart defects in Down syndrome. American Journal of Medical Genetics. 80: 213-7. PMID 9843040 DOI: 10.1002/(SICI)1096-8628(19981116)80:3<213::AID-AJMG6>3.0.CO;2-8  0.32
1998 Zaragoza MV, Millie E, Redline RW, Hassold TJ. Studies of non-disjunction in trisomies 2, 7, 15, and 22: does the parental origin of trisomy influence placental morphology? Journal of Medical Genetics. 35: 924-31. PMID 9832040  0.32
1998 Shaffer LG, McCaskill C, Adkins K, Hassold TJ. Systematic search for uniparental disomy in early fetal losses: the results and a review of the literature. American Journal of Medical Genetics. 79: 366-72. PMID 9779803 DOI: 10.1002/(SICI)1096-8628(19981012)79:5<366::AID-AJMG7>3.0.CO;2-H  0.32
1998 Redline RW, Hassold T, Zaragoza M. Determinants of villous trophoblastic hyperplasia in spontaneous abortions Modern Pathology. 11: 762-768. PMID 9720505  0.32
1998 Savage AR, Petersen MB, Pettay D, Taft L, Allran K, Freeman SB, Karadima G, Avramopoulos D, Torfs C, Mikkelsen M, Hassold TJ, Sherman SL. Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans. Human Molecular Genetics. 7: 1221-7. PMID 9668162  0.32
1998 Shen JJ, Sherman SL, Hassold TJ. Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome Chromosoma. 107: 166-172. PMID 9639654 DOI: 10.1007/s004120050293  0.32
1998 Redline RW, Hassold T, Zaragoza MV. Prevalence of the partial molar phenotype in triploidy of maternal and paternal origin Human Pathology. 29: 505-511. PMID 9596275 DOI: 10.1016/S0046-8177(98)90067-3  0.32
1998 Robinson WP, Kuchinka BD, Bernasconi F, Petersen MB, Schulze A, Brondum-Nielsen K, Christian SL, Ledbetter DH, Schinzel AA, Horsthemke B, Schuffenhauer S, Michaelis RC, Langlois S, Hassold TJ. Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination. Human Molecular Genetics. 7: 1011-9. PMID 9580665 DOI: 10.1093/Hmg/7.6.1011  0.32
1998 Hassold TJ. Nondisjunction in the human male Current Topics in Developmental Biology. 37: 383-406. PMID 9352193  0.32
1997 O'Keefe CL, Griffin DK, Bean CJ, Matera AG, Hassold TJ. Alphoid variant-specific FISH probes can distinguish autosomal meiosis I from meiosis II non-disjunction in human sperm. Human Genetics. 101: 61-6. PMID 9385371 DOI: 10.1007/S004390050587  0.32
1997 Griffin DK, Millie EA, Redline RW, Hassold TJ, Zaragoza MV. Cytogenetic analysis of spontaneous abortions: comparison of techniques and assessment of the incidence of confined placental mosaicism. American Journal of Medical Genetics. 72: 297-301. PMID 9332658 DOI: 10.1002/(SICI)1096-8628(19971031)72:3<297::AID-AJMG9>3.0.CO;2-O  0.32
1997 Lamb NE, Feingold E, Savage A, Avramopoulos D, Freeman S, Gu Y, Hallberg A, Hersey J, Karadima G, Pettay D, Saker D, Shen J, Taft L, Mikkelsen M, Petersen MB, ... Hassold T, et al. Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21 Human Molecular Genetics. 6: 1391-1399. PMID 9285774 DOI: 10.1093/Hmg/6.9.1391  0.32
1997 Zaragoza MV, Keep D, Genest DR, Hassold T, Redline RW. Early complete hydatidiform moles contain inner cell mass derivatives. American Journal of Medical Genetics. 70: 273-7. PMID 9188665 DOI: 10.1002/(Sici)1096-8628(19970613)70:3<273::Aid-Ajmg11>3.0.Co;2-I  0.32
1996 Lamb NE, Freeman SB, Savage-Austin A, Pettay D, Taft L, Hersey J, Gu Y, Shen J, Saker D, May KM, Avramopoulos D, Petersen MB, Hallberg A, Mikkelsen M, Hassold TJ, et al. Susceptible chiasmate configurations of chromosome 21 predispose to non- disjunction in both maternal meiosis I and meiosis II Nature Genetics. 14: 400-405. PMID 8944019 DOI: 10.1038/ng1296-400  0.32
1996 Hassold T, Abruzzo M, Adkins K, Griffin D, Merrill M, Millie E, Saker D, Shen J, Zaragoza M. Human aneuploidy: incidence, origin, and etiology. Environmental and Molecular Mutagenesis. 28: 167-75. PMID 8908177 DOI: 10.1002/(Sici)1098-2280(1996)28:3<167::Aid-Em2>3.0.Co;2-B  0.32
1996 Bishop JB, Dellarco VL, Hassold T, Ferguson LR, Wyrobek AJ, Friedman JM. Aneuploidy in germ cells: etiologies and risk factors. Environmental and Molecular Mutagenesis. 28: 159-66. PMID 8908176 DOI: 10.1002/(Sici)1098-2280(1996)28:3<159::Aid-Em1>3.0.Co;2-9  0.32
1996 Griffin DK, Abruzzo MA, Millie EA, Feingold E, Hassold TJ. Sex ratio in normal and disomic sperm: evidence that the extra chromosome 21 preferentially segregates with the Y chromosome. American Journal of Human Genetics. 59: 1108-13. PMID 8900240  0.32
1996 Koehler KE, Hawley RS, Sherman S, Hassold T. Recombination and nondisjunction in humans and flies. Human Molecular Genetics. 5: 1495-504. PMID 8875256 DOI: 10.1093/Hmg/5.Supplement_1.1495  0.32
1996 Keep D, Zaragoza MV, Hassold T, Redline RW. Very early complete hydatidiform mole Human Pathology. 27: 708-713. PMID 8698316 DOI: 10.1016/S0046-8177(96)90402-5  0.32
1996 Hassold TJ. Mismatch repair goes meiotic Nature Genetics. 13: 261-263. PMID 8673119 DOI: 10.1038/ng0796-261  0.32
1996 Yoon PW, Freeman SB, Sherman SL, Taft LF, Gu Y, Pettay D, Flanders WD, Khoury MJ, Hassold TJ. Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study. American Journal of Human Genetics. 58: 628-33. PMID 8644722  0.32
1996 Abruzzo MA, Griffin DK, Millie EA, Sheean LA, Hassold TJ. The effect of Y-chromosome alpha-satellite array length on the rate of sex chromosome disomy in human sperm Human Genetics. 97: 819-823. PMID 8641703 DOI: 10.1007/s004390050143  0.32
1995 Griffin DK, Abruzzo MA, Millie EA, Sheean LA, Feingold E, Sherman SL, Hassold TJ. Non-disjunction in human sperm: Evidence for an effect of increasing paternal age Human Molecular Genetics. 4: 2227-2232. PMID 8634691 DOI: 10.1093/Hmg/4.12.2227  0.32
1995 Hassold T, Sherman S, Hunt PA. The origin of trisomy in humans Progress in Clinical and Biological Research. 393: 1-12. PMID 8545442  0.32
1995 Abruzzo MA, Hassold TJ. Etiology of nondisjunction in humans Environmental and Molecular Mutagenesis. 25: 38-47. PMID 7789361 DOI: 10.1002/em.2850250608  0.32
1995 Shen JJ, Williams BJ, Zipursky A, Doyle J, Sherman SL, Jacobs PA, Shugar AL, Soukup SW, Hassold TJ. Cytogenetic and molecular studies of Down syndrome individuals with leukemia. American Journal of Human Genetics. 56: 915-25. PMID 7717402  0.32
1995 Hassold T, Merrill M, Adkins K, Freeman S, Sherman S. Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16. American Journal of Human Genetics. 57: 867-74. PMID 7573048  0.32
1995 Jacobs PA, Hassold TJ. 4 The Origin of Numerical Chromosome Abnormalities Advances in Genetics. 33: 101-133. PMID 7484451 DOI: 10.1016/S0065-2660(08)60332-6  0.32
1994 James RS, Temple IK, Patch C, Thompson EM, Hassold T, Jacobs PA. A systematic search for uniparental disomy in carriers of chromosome translocations. European Journal of Human Genetics : Ejhg. 2: 83-95. PMID 8044660  0.32
1994 Macdonald M, Hassold T, Harvey J, Wang LH, Morton NE, Jacobs P. The origin of 47, XXY and 47, XXX aneuploidy: Heterogeneous mechanisms and role of aberrant recombination Human Molecular Genetics. 3: 1365-1371. PMID 7987316 DOI: 10.1093/Hmg/3.8.1365  0.32
1994 Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherman S, Hassold T. Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns Human Genetics. 94: 411-417. PMID 7927339 DOI: 10.1007/Bf00201603  0.32
1994 Sherman SL, Petersen MB, Freeman SB, Hersey J, Pettay D, Taft L, Frantzen M, Mikkelsen M, Hassold TJ. Non-disjunction of chromosome 21 in maternal meiosis I: Evidence for a maternal age-dependent mechanism involving reduced recombination Human Molecular Genetics. 3: 1529-1535. PMID 7833907 DOI: 10.1093/hmg/3.9.1529  0.32
1993 Freeman SB, May KM, Pettay D, Fernhoff PM, Hassold TJ. Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndrome. American Journal of Medical Genetics. 45: 625-30. PMID 8456836 DOI: 10.1002/ajmg.1320450522  0.32
1993 Hassold T, Hunt PA, Sherman S. Trisomy in humans: incidence, origin and etiology Current Opinion in Genetics and Development. 3: 398-403. PMID 8353412 DOI: 10.1016/0959-437X(93)90111-2  0.32
1993 Williams BJ, Ballenger CA, Malter HE, Bishop F, Tucker M, Zwingman TA, Hassold TJ. Non-disjunction in human sperm: results of fluorescence in situ hybridization studies using two and three probes. Human Molecular Genetics. 2: 1929-36. PMID 8281157 DOI: 10.1093/hmg/2.11.1929  0.32
1993 Patersen MB, Antonarakis SE, Hassold TJ, Freeman SB, Sherman SL, Avramopoulos D, Mikkelsen M. Paternal nondisjunction in trisomy 21: Excess of male patients Human Molecular Genetics. 2: 1691-1695. PMID 8268923 DOI: 10.1093/hmg/2.10.1691  0.32
1992 Krasikov N, Takaesu N, Hassold T, Knops JF, Finley WH, Scarbrough P. Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype. American Journal of Medical Genetics. 43: 554-60. PMID 1605248 DOI: 10.1002/Ajmg.1320430310  0.32
1992 Lorber BJ, Grantham M, Peters J, Willard HF, Hassold TJ. Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin. American Journal of Human Genetics. 51: 1265-76. PMID 1463010  0.32
1992 Lorber BJ, Freeman SB, Hassold T, Ragab AH, Vega RA, Cockwell AE, Jacobs PA, Radford M, Doyle J, Dubé ID. Characterization and molecular analysis of nondisjunction in 18 cases of trisomy 21 and leukemia. Genes, Chromosomes & Cancer. 4: 222-7. PMID 1382563 DOI: 10.1002/Gcc.2870040306  0.32
1992 Takaesu N, Newfeld S, Hassold T. Characterization of three VNTR systems at D21S112 Genomics. 14: 816-817. PMID 1339394 DOI: 10.1016/S0888-7543(05)80197-1  0.32
1991 Hassold TJ, Pettay D, Freeman SB, Grantham M, Takaesu N. Molecular studies of non-disjunction in trisomy 16. Journal of Medical Genetics. 28: 159-62. PMID 2051452  0.32
1991 Hassold TJ, Sherman SL, Pettay D, Page DC, Jacobs PA. XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region American Journal of Human Genetics. 49: 253-260. PMID 1867189  0.32
1991 Sherman SL, Takaesu N, Freeman SB, Grantham M, Phillips C, Blackston RD, Jacobs PA, Cockwell AE, Freeman V, Uchida I, Mikkelsen M, Kurnit DM, Buraczynska M, Keats BJB, Hassold TJ. Trisomy 21: Association between reduced recombination and nondisjunction American Journal of Human Genetics. 49: 608-620. PMID 1831960  0.32
1991 Temple IK, Cockwell A, Hassold T, Pettay D, Jacobs P. Maternal uniparental disomy for chromosome 14. Journal of Medical Genetics. 28: 511-4. PMID 1681108  0.32
1990 May KM, Jacobs PA, Lee M, Ratcliffe S, Robinson A, Nielsen J, Hassold TJ. The parental origin of the extra X chromosome in 47,XXX females. American Journal of Human Genetics. 46: 754-61. PMID 2316522  0.32
1990 Harvey J, Jacobs PA, Hassold T, Pettay D. The parental origin of 47,XXY males Birth Defects: Original Article Series. 26: 289-296. PMID 2090327  0.32
1990 Hassold T, Arnovitz K, Jacobs PA, May K, Robinson D. The parental origin of the missing or additional chromosome in 45,X and 47,XXX females Birth Defects: Original Article Series. 26: 297-304. PMID 1982521  0.32
1990 Takaesu N, Jacobs PA, Cockwell A, Blackston RD, Freeman S, Nuccio J, Kurnit DM, Uchida I, Freeman V, Hassold T. Nondisjunction of chromosome 21. American Journal of Medical Genetics. Supplement. 7: 175-81. PMID 1981476 DOI: 10.1002/Ajmg.1320370735  0.32
1990 Morton NE, Keats BJ, Jacobs PA, Hassold T, Pettay D, Harvey J, Andrews V. A centromere map of the X chromosome from trisomies of maternal origin Annals of Human Genetics. 54: 39-47. PMID 1969722 DOI: 10.1111/J.1469-1809.1990.Tb00359.X  0.32
1989 Hassold TJ, Takaesu N. Analysis of non-disjunction in human trisomic spontaneous abortions Progress in Clinical and Biological Research. 311: 115-134. PMID 2570425  0.32
1989 Buraczynska M, Stewart GD, Sherman S, Freeman V, Grantham M, Uchida I, Hassold T, Kurnit DM. Studying nondisjunction of chromosome 21 with cytogenetic markers on the short arm and DNA markers encompassing the long arm Progress in Clinical and Biological Research. 311: 101-113. PMID 2570424  0.32
1989 Jacobs P, Hassold T, Harvey J, May K. The origin of sex chromosome aneuploidy Progress in Clinical and Biological Research. 311: 135-151. PMID 2528150  0.32
1989 Harbison M, Hassold T, Kobryn C, Jacobs PA. Molecular studies of the parental origin and nature of human X lsochromosomes Obstetrical and Gynecological Survey. 44: 690-691.  0.32
1988 Hassold T, Jacobs PA, Pettay D. Cytogenetic studies of couples with repeated spontaneous abortions of known karyotype Genetic Epidemiology. 5: 65-74. PMID 3402725  0.32
1988 Jacobs PA, Bacino C, Hassold T, Morton NE, Keston M, Lee M. A cytogenetic study of 47,XXY males of known origin and their parents Annals of Human Genetics. 52: 319-325. PMID 3268043 DOI: 10.1111/J.1469-1809.1988.Tb01111.X  0.32
1988 Morton NE, Jacobs PA, Hassold T, Wu D. Maternal age in trisomy Annals of Human Genetics. 52: 227-235. PMID 2977936 DOI: 10.1111/J.1469-1809.1988.Tb01100.X  0.32
1988 Stewart GD, Hassold TJ, Kurnit DM. Trisomy 21. Molecular and cytogenetic studies of nondisjunction Advances in Human Genetics. 17: 99-140. PMID 2973207  0.32
1988 Jacobs PA, Hassold TJ, Whittington E, Butler G, Collyer S, Keston M, Lee M. Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes. Annals of Human Genetics. 52: 93-109. PMID 2907853  0.32
1988 Harbison M, Hassold T, Kobryn C, Jacobs PA. Molecular studies of the parental origin and nature of human X isochromosomes Cytogenetics and Cell Genetics. 47: 217-222. PMID 2901328  0.32
1988 Hassold T, Benham F, Leppert M. Cytogenetic and molecular analysis of sex-chromosome monosomy. American Journal of Human Genetics. 42: 534-41. PMID 2894760  0.32
1988 Stewart GD, Hassold TJ, Berg A, Watkins P, Tanzi R, Kurnit DM. Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21. American Journal of Human Genetics. 42: 227-36. PMID 2893544  0.32
1987 Warburton D, Kline J, Stein Z, Hutzler M, Chin A, Hassold T. Does the karyotype of a spontaneous abortion predict the karyotype of a subsequent abortion? Evidence from 273 women with two karyotyped spontaneous abortions. American Journal of Human Genetics. 41: 465-83. PMID 3631080  0.32
1987 Hassold T, Jacobs PA, Pettay D. Analysis of nucleolar organizing regions in parents of trisomic spontaneous abortions Human Genetics. 76: 381-384. PMID 3610159 DOI: 10.1007/BF00272449  0.32
1987 Jacobs PA, Hassold TJ, Henry A, Pettay D, Takaesu N. Trisomy 13 ascertained in a survey of spontaneous abortions. Journal of Medical Genetics. 24: 721-4. PMID 3430552  0.32
1987 Hassold T, Jacobs PA, Leppert M, Sheldon M. Cytogenetic and molecular studies of trisomy 13. Journal of Medical Genetics. 24: 725-32. PMID 2892938  0.32
1986 Hassold TJ. Chromosome abnormalities in human reproductive wastage Trends in Genetics. 2: 105-110. DOI: 10.1016/0168-9525(86)90194-0  0.32
1985 Hassold T, Chiu D. Maternal age-specific rates of numerical chromosome abnormalities with special reference to trisomy Human Genetics. 70: 11-17. PMID 3997148 DOI: 10.1007/Bf00389450  0.32
1985 Hassold TJ. The origin of aneuploidy in humans Basic Life Sciences. 36: 103-115. PMID 3006652  0.32
1985 Hassold T, Kumlin E, Takaesu N, Leppert M. Determination of the parental origin of sex-chromosome monosomy using restriction fragment length polymorphisms. American Journal of Human Genetics. 37: 965-72. PMID 2996336  0.32
1985 Hassold T, Kumlin E, Takaesu N, Leppert M. Use of restriction fragment length polymorphisms to study the origin of human aneuploidy Annals of the New York Academy of Sciences. 179-189. PMID 2990309 DOI: 10.1111/J.1749-6632.1985.Tb21492.X  0.32
1984 Hassold T, MacLean C. Temporal changes in chromosome abnormality rate in human spontaneous abortions: Evidence for an association between sex-chromosome monosomy and trisomy 16 Cytogenetics and Cell Genetics. 38: 200-205. PMID 6541559  0.32
1984 Hassold T, Warburton D, Kline J, Stein Z. The relationship of maternal age and trisomy among trisomic spontaneous abortions. American Journal of Human Genetics. 36: 1349-56. PMID 6517056  0.32
1984 Hassold TJ, Jacobs PA. Trisomy in man Annual Review of Genetics. 18: 69-97. PMID 6241455  0.32
1984 Hassold T, Chiu D, Yamane JA. Parental origin of autosomal trisomies Annals of Human Genetics. 48: 129-144. PMID 6234852 DOI: 10.1111/J.1469-1809.1984.Tb01008.X  0.32
1983 Hassold T, Sandison A. The effect of chromosome constitution on growth in culture of human spontaneous abortions Human Genetics. 63: 166-170. PMID 6840759 DOI: 10.1007/Bf00291538  0.32
1983 Hassold T, Quillen SD, Yamane JA. Sex ratio in spontaneous abortions Annals of Human Genetics. 47: 39-47. PMID 6838169 DOI: 10.1111/J.1469-1809.1983.Tb00968.X  0.32
1982 Hassold T. Mosaic trisomies in human spontaneous abortions Human Genetics. 61: 31-35. PMID 7129422 DOI: 10.1007/BF00291327  0.32
1982 Morton NE, Hassold TJ, Funkhouser J, McKenna PW, Lew R. Cytogenetic surveillance of spontaneous abortions Cytogenetic and Genome Research. 33: 232-239. PMID 7128213 DOI: 10.1159/000131759  0.32
1980 Hassold TJ. A cytogenetic study of repeated spontaneous abortions. American Journal of Human Genetics. 32: 723-30. PMID 7424911  0.32
1980 Hassold T, Chen N, Funkhouser J, Jooss T, Manuel B, Matsuura J, Matsuyama A, Wilson C, Yamane JA, Jacobs PA. A cytogenetic study of 1000 spontaneous abortions Annals of Human Genetics. 44: 151-178. PMID 7316468 DOI: 10.1111/J.1469-1809.1980.Tb00955.X  0.32
1980 Hassold T, Jacobs P, Kline J, Stein Z, Warburton D. Effect of maternal age on autosomal trisomies Annals of Human Genetics. 44: 29-36. PMID 7198887 DOI: 10.1111/J.1469-1809.1980.Tb00943.X  0.32
1979 Wisniewski L, Hassold T, Heffelfinger J, Higgins JV. Cytogenetic and clinical studies in five cases of inv dup(15) Human Genetics. 50: 259-270. PMID 489010 DOI: 10.1007/Bf00399391  0.32
1979 Hassold T, Matsuyama A. Origin of trisomies in human spontaneous abortions Human Genetics. 46: 285-294. PMID 155642 DOI: 10.1007/BF00273312  0.32
1978 Jacobs PA, Angell RR, Buchanan IM, Hassold TJ, Matsuyama AM, Manuel B. The origin of human triploids Annals of Human Genetics. 42: 49-57. PMID 686684  0.32
1978 Hassold TJ, Matsuyama A, Newlands IM, Matsuura JS, Jacobs PA, Manuel B, Tsuei J. A cytogenetic study of spontaneous abortions in Hawaii Annals of Human Genetics. 41: 443-454. PMID 655633  0.32
1977 Wisniewski L, Purdy G, Hassold T, Wilson C, Bentley K, Hackel E, Higgins JV. An interstitial deletion of chromosome 9 in a girl with multiple congenital anomalies. Journal of Medical Genetics. 14: 455-9. PMID 604498 DOI: 10.1136/Jmg.14.6.455  0.32
1977 Hassold T, Slatis HM, Berker I. Detection of new chromosome malformation syndromes through a dermatoglyphic screen of a mentally retarded population Birth Defects: Original Article Series. 13: 237-238.  0.32
1976 Higgins JV, Wisniewski L, Hassold T, Hackel E, Raeburn RA, Buckton KE, Noades JE, Cook PJ. Two informative translocations involving chromosome 2 HUMAN GENE MAPPING.3 Birth Defects: Original Article Series. 12: 314-316. PMID 1088255  0.32
1976 Higgins JV, Wisniewski L, Hassold T, Hackel E, Raeburn RA, Buckton KE, Noades JE, Cook P. Two informative translocations involving chromosome 2 Cytogenetic and Genome Research. 16: 314-316. PMID 975898 DOI: 10.1159/000130619  0.32
1976 Hassold TJ, Slatis HM. The detection of abnormalities through rare fingerprint combinations | FIFTH INTERNATIONAL CONGRESS OF HUMAN GENETICS Excerpta Med.,Amsterdam,I.C.S.. No.528.  0.32
1976 Wisniewski L, Purdy G, Hassold T. The secondary constriction of chromosome 9: deletion and breakage studies Excerpta Med.,Amsterdam,I.C.S. 0.32
1976 Leonard M, Wisniewski L, Hassold T. A familial 2/4 translocation: cytogenetic and linkage studies Excerpta Med.,Amsterdam,I.C.S. 0.32
1976 Warren ST, Hassold TJ, Slatis HM. Dermatoglyphic abnormalities associated with mucopolysaccharide disorders | FIFTH INTERNATIONAL CONGRESS OF HUMAN GENETICS Excerpta Med.,Amsterdam,I.C.S.. No.559.  0.32
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