Year |
Citation |
Score |
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 |
0.347 |
|
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 |
0.308 |
|
2002 |
Linden MG, Bender BG, Robinson A. Genetic counseling for sex chromosome abnormalities. American Journal of Medical Genetics. 110: 3-10. PMID 12116264 DOI: 10.1002/Ajmg.10391 |
0.328 |
|
1996 |
Linden MG, Bender BG, Robinson A. Intrauterine diagnosis of sex chromosome aneuploidy Obstetrics & Gynecology. 87: 468-475. PMID 8598978 DOI: 10.1016/0029-7844(95)00419-X |
0.365 |
|
1991 |
Bender BG, Linden M, Robinson A. Cognitive and academic skills in children with sex chromosome abnormalities Reading and Writing. 3: 127-139. DOI: 10.1007/Bf00354965 |
0.351 |
|
1987 |
Morse HG, Odom LF, Castro R, Hays T, Blake M, Vannais D, Robinson A. Methodology of premature chromosome condensation and its potential for relapse prediction in acute leukemia of children and adolescents. Cancer Genetics and Cytogenetics. 27: 51-61. PMID 3581041 DOI: 10.1016/0165-4608(87)90260-3 |
0.315 |
|
1982 |
Pennington BF, Bender B, Puck M, Salbenblatt J, Robinson A. Learning disabilities in children with sex chromosome anomalies. Child Development. 53: 1182-92. PMID 7140426 DOI: 10.1111/J.1467-8624.1982.Tb04155.X |
0.307 |
|
1982 |
Morse HG, Hays T, Patterson D, Robinson A. Giemsa-11 technique. Applications in the chromosomal characterization of hematologic specimens. Human Genetics. 61: 141-144. PMID 6957375 DOI: 10.1007/Bf00274204 |
0.341 |
|
1981 |
Sujansky E, Smith ACM, Peakman DC, McConnell TS, Baca P, Robinson A, Opitz JM. Familial pericentric inversion of chromosome 8. American Journal of Medical Genetics. 10: 229-235. PMID 6171164 DOI: 10.1002/Ajmg.1320100305 |
0.364 |
|
1979 |
Hecht F, McCaw BK, Peakman D, Robinson A. New translocations in human lymphocytes: A mutagen monitoring system Environmental Health Perspectives. 19-22. PMID 499124 DOI: 10.1289/Ehp.793119 |
0.353 |
|
1979 |
Hays T, Morse H, Peakman D, Rose B, Robinson A. Cytogenetic studies of chronic myelocytic leukemia in children and adolescents. Cancer. 44: 210-214. PMID 287550 DOI: 10.1002/1097-0142(197907)44:1<210::Aid-Cncr2820440134>3.0.Co;2-Y |
0.327 |
|
1979 |
Morse H, Hays T, Peakman D, Rose B, Robinson A. Acute nonlymphoblastic leukemia in childhood. High incidence of clonal abnormalities and nonrandom changes Cancer. 44: 164-170. PMID 287549 DOI: 10.1002/1097-0142(197907)44:1<164::Aid-Cncr2820440128>3.0.Co;2-9 |
0.345 |
|
1974 |
Robinson A. Letter: Neonatal deaths and sex-chromosome anomalies Lancet. 1: 1223. PMID 4134690 DOI: 10.1016/S0140-6736(74)91029-0 |
0.327 |
|
1974 |
Robinson A, Puck M, Tennes K. The 47,Xxy Karyotype The Lancet. 303: 1343. PMID 4134316 DOI: 10.1016/S0140-6736(74)90708-9 |
0.343 |
|
1974 |
Robinson A, Puck M, Tennes K, Bryant K. Early Childhood Development Of Four Boys With 47,Xxy Karyotype Pediatric Research. 8: 394-394. DOI: 10.1203/00006450-197404000-00326 |
0.357 |
|
1967 |
Robinson A, Goad WB, Puck TT, Harris JS. Studies On Chromosomal Nondisjunction In Man. Iii Obstetrical & Gynecological Survey. 22: 350-352. DOI: 10.1097/00006254-196706000-00027 |
0.34 |
|
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