Catherine Gardella Palmer - Publications

1994 Medical Genetics Indiana University, Bloomington, Bloomington, IN, United States 
medical genetics

63 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
2015 Nagakura H, Schneider G, Morris J, Lafferty KA, Palmer CG. Assessing deaf awareness training: knowledge and attitudes of recent genetic counseling graduates. Journal of Genetic Counseling. 24: 104-16. PMID 25030269 DOI: 10.1007/s10897-014-9742-3  0.01
2015 Schully SD, Lam TK, Dotson WD, Chang CQ, Aronson N, Birkeland ML, Brewster SJ, Boccia S, Buchanan AH, Calonge N, Calzone K, Djulbegovic B, Goddard KA, Klein RD, Klein TE, ... Palmer CG, et al. Evidence synthesis and guideline development in genomic medicine: current status and future prospects. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 63-7. PMID 24946156 DOI: 10.1038/Gim.2014.69  0.01
2014 Palmer CG, Boudreault P, Baldwin EE, Sinsheimer JS. Impact of genetic counseling and Connexin-26 and Connexin-30 testing on deaf identity and comprehension of genetic test results in a sample of deaf adults: a prospective, longitudinal study. Plos One. 9: e111512. PMID 25375116 DOI: 10.1371/Journal.Pone.0111512  0.01
2014 Roche MI, Palmer CG. Next generation genetic counseling: introduction to the special issue. Journal of Genetic Counseling. 23: 439-44. PMID 24838698 DOI: 10.1007/s10897-014-9729-0  0.01
2014 Alford RL, Arnos KS, Fox M, Lin JW, Palmer CG, Pandya A, Rehm HL, Robin NH, Scott DA, Yoshinaga-Itano C. American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 347-55. PMID 24651602 DOI: 10.1038/Gim.2014.2  0.01
2013 Kobayashi Y, Boudreault P, Hill K, Sinsheimer JS, Palmer CG. Using a social marketing framework to evaluate recruitment of a prospective study of genetic counseling and testing for the deaf community. Bmc Medical Research Methodology. 13: 145. PMID 24274380 DOI: 10.1186/1471-2288-13-145  0.01
2010 Resta RG, McCarthy Veach P, Charles S, Vogel K, Blase T, Palmer CG. Publishing a master's thesis: a guide for novice authors. Journal of Genetic Counseling. 19: 217-27. PMID 20076994 DOI: 10.1007/S10897-009-9276-2  0.01
1999 Park JP, Brothman AR, Butler MG, Cooley LD, Dewald GW, Lundquist KF, Palmer CG, Patil SR, Rao KW, Saikevych IA, Schneider NR, Vance GH. Extensive analysis of mosaicism in a case of Turner syndrome: the experience of 287 cytogenetic laboratories. College of American Pathologists/American College of Medical Genetics Cytogenetics Resource Committee. Archives of Pathology & Laboratory Medicine. 123: 381-5. PMID 10235494 DOI: 10.1043/0003-9985(1999)123<0381:EAOMIA>2.0.CO;2  1
1999 Smolarek TA, Blough RI, Foster RS, Ulbright TM, Palmer CG, Heerema NA. Cytogenetic analyses of 85 testicular germ cell tumors: comparison of postchemotherapy and untreated tumors. Cancer Genetics and Cytogenetics. 108: 57-69. PMID 9973926 DOI: 10.1016/S0165-4608(98)00113-7  1
1998 Vance GH, Nickerson C, Sarnat L, Zhang A, Henegariu O, Morichon-Delvallez N, Butler MG, Palmer CG. Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q. American Journal of Medical Genetics. 76: 51-7. PMID 9508065 DOI: 10.1002/(Sici)1096-8628(19980226)76:1<51::Aid-Ajmg9>3.0.Co;2-S  1
1997 Vance GH, Curtis CA, Heerema NA, Schwartz S, Palmer CG. An apparently acentric marker chromosome originating from 9p with a functional centromere without detectable alpha and beta satellite sequences. American Journal of Medical Genetics. 71: 436-42. PMID 9286452 DOI: 10.1002/(Sici)1096-8628(19970905)71:4<436::Aid-Ajmg13>3.0.Co;2-H  1
1997 Henegariu O, Kernek S, Keating MA, Palmer CG, Heerema NA. PCR and FISH analysis of a ring Y chromosome. American Journal of Medical Genetics. 69: 171-6. PMID 9056556 DOI: 10.1002/(Sici)1096-8628(19970317)69:2<171::Aid-Ajmg11>3.0.Co;2-I  1
1997 Zhang A, Weaver DD, Palmer CG. Molecular cytogenetic identification of four X chromosome duplications. American Journal of Medical Genetics. 68: 29-38. PMID 8986272 DOI: 10.1002/(Sici)1096-8628(19970110)68:1<29::Aid-Ajmg6>3.0.Co;2-T  1
1996 Sun Y, Nicholls RD, Butler MG, Saitoh S, Hainline BE, Palmer CG. Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient. Human Molecular Genetics. 5: 517-24. PMID 8845846 DOI: 10.1093/Hmg/5.4.517  1
1995 Smolarek TA, Blough RI, Foster RS, Ulbright TM, Palmer CG, Heerema NA. Identification of multiple chromosome 12 abnormalities in human testicular germ cell tumors by two-color fluorescence in situ hybridization (FISH). Genes, Chromosomes & Cancer. 14: 252-8. PMID 8605113 DOI: 10.1002/Gcc.2870140403  1
1995 Hainline BE, Padilla LM, Chong SK, Heifetz SA, Palmer C, Zhou FC. Fetal tissue derived from spontaneous pregnancy losses is insufficient for human transplantation. Obstetrics and Gynecology. 85: 619-24. PMID 7898844 DOI: 10.1016/0029-7844(95)00003-A  1
1995 Wheeler PG, Weaver DD, Palmer CG. Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome. American Journal of Medical Genetics. 55: 462-5. PMID 7762587 DOI: 10.1002/Ajmg.1320550414  1
1995 Harmon JP, Hiett AK, Palmer CG, Golichowski AM. Prenatal ultrasound detection of isolated neural tube defects: is cytogenetic evaluation warranted? Obstetrics and Gynecology. 86: 595-9. PMID 7675386 DOI: 10.1016/S0029-7844(95)80023-9  1
1995 Palmer CG, Blouin JL, Bull MJ, Breitfeld P, Vance GH, Van Meter T, Weaver DD, Heerema NA, Colbern SG, Korenberg JR. Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemia. American Journal of Medical Genetics. 57: 527-36. PMID 7573123 DOI: 10.1002/Ajmg.1320570403  1
1995 Sun Y, Rubinstein J, Soukup S, Palmer CG. Marker chromosome 21 identified by microdissection and FISH. American Journal of Medical Genetics. 56: 151-4. PMID 7542834 DOI: 10.1002/Ajmg.1320560207  1
1994 Leana-Cox J, Jenkins L, Palmer CG, Plattner R, Sheppard L, Flejter WL, Zackowski J, Tsien F, Schwartz S. Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications. American Journal of Human Genetics. 54: 748-56. PMID 8178816  1
1994 Mewar R, Harrison W, Weaver DD, Palmer C, Davee MA, Overhauser J. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype. American Journal of Medical Genetics. 52: 178-83. PMID 7802005 DOI: 10.1002/Ajmg.1320520211  1
1993 Plattner R, Heerema NA, Yurov YB, Palmer CG. Efficient identification of marker chromosomes in 27 patients by stepwise hybridization with alpha-satellite DNA probes Human Genetics. 91: 131-140. PMID 8462972 DOI: 10.1007/Bf00222713  1
1993 Hoeltge GA, Dewald G, Palmer CG, David-Nelson MA, Saikevych I, Patil S, Schwartz S, Schneider NR, Herrmann M. Proficiency testing in clinical cytogenetics. A 6-year experience with photographs, fixed cells, and fresh blood. Archives of Pathology & Laboratory Medicine. 117: 776-9. PMID 8343040  1
1993 Plattner R, Heerema NA, Howard-Peebles PN, Miles JH, Soukup S, Palmer CG. Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization. Human Genetics. 91: 589-98. PMID 8340114 DOI: 10.1007/Bf00205086  1
1993 Reilly PA, Heerema NA, Sledge GW, Palmer CG. Unusual distribution of chromosome 12 in a testicular germ-cell tumor cell line (833K) and its cisplatin-resistant derivative (64CP9). Cancer Genetics and Cytogenetics. 68: 114-21. PMID 7689033 DOI: 10.1016/0165-4608(93)90006-8  1
1992 Heerema NA, Palmer CG, Weetman R, Bertolone S. Cytogenetic analysis in relapsed childhood acute lymphoblastic leukemia. Leukemia. 6: 185-92. PMID 1564954  1
1992 Lowe LR, Heerema NA, Cheerva AC, Palmer CG. A new nonrandom chromosomal abnormality, t(2;16)(p11.2;p11.2), possibly associated with poor outcome in childhood acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 64: 60-4. PMID 1458451 DOI: 10.1016/0165-4608(92)90324-2  1
1992 Van Dyke DL, Wiktor A, Palmer CG, Miller DA, Witt M, Babu VR, Worsham MJ, Roberson JR, Weiss L. Ullrich-Turner syndrome with a small ring X chromosome and presence of mental retardation. American Journal of Medical Genetics. 43: 996-1005. PMID 1415351 DOI: 10.1002/ajmg.1320430617  1
1991 Palmer CG, Bader P, Slovak ML, Comings DE, Pettenati MJ. Partial deletion of chromosome 6p: delineation of the syndrome. American Journal of Medical Genetics. 39: 155-60. PMID 2063917 DOI: 10.1002/Ajmg.1320390208  0.01
1991 Plattner R, Heerema NA, Patil SR, Howard-Peebles PN, Palmer CG. Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization. Human Genetics. 87: 290-6. PMID 1864603 DOI: 10.1007/Bf00200906  1
1990 Palmer CG, Heerema N, Bull M. Deletions in chromosome 2 and fragile sites. American Journal of Medical Genetics. 36: 214-8. PMID 2368809 DOI: 10.1002/ajmg.1320360215  1
1990 Milatovich A, Heerema NA, Palmer CG. Cytogenetic studies of endometrial malignancies. Cancer Genetics and Cytogenetics. 46: 41-53. PMID 2331682 DOI: 10.1016/0165-4608(90)90007-W  1
1989 Fekete G, Plattner R, Crabb DW, Zhang B, Harris RA, Heerema N, Palmer CG. Localization of the human gene for the El alpha subunit of branched chain keto acid dehydrogenase (BCKDHA) to chromosome 19q13.1----q13.2. Cytogenetics and Cell Genetics. 50: 236-7. PMID 2805821 DOI: 10.1159/000132768  1
1988 Rao PN, Heerema NA, Palmer CG. Expression of fragile sites in childhood acute lymphoblastic leukemia patients and normal controls. Human Genetics. 79: 329-34. PMID 2970424 DOI: 10.1007/Bf00282170  1
1988 Rao PN, Heerema NA, Palmer CG. Fragile sites induced by FUdR, caffeine, and aphidicolin. Their frequency, distribution, and analysis. Human Genetics. 78: 21-6. PMID 2962925 DOI: 10.1007/Bf00291228  1
1988 Milatovich A, Plattner R, Heerema NA, Palmer CG, Lopez-Casillas F, Kim KH. Localization of the gene for acetyl-CoA carboxylase to human chromosome 17. Cytogenetics and Cell Genetics. 48: 190-2. PMID 2906852 DOI: 10.1159/000132623  1
1987 Goldstein DJ, Ward RE, Nichols WC, Palmer CG. Familial t(8;15)(p23·3;q22·3): report of two cases with dup(15)(q22·3→qter) Journal of Medical Genetics. 24: 684-687. PMID 3430543 DOI: 10.1136/jmg.24.11.684  1
1987 Palmer CG, Miles JH, Howard-Peebles PN, Magenis RE, Patil S, Friedman JM. Fetal karyotype following ascertainment of fetal anomalies by ultrasound. Prenatal Diagnosis. 7: 551-5. PMID 3317386 DOI: 10.1002/Pd.1970070804  1
1987 Nichols CR, Heerema NA, Palmer C, Loehrer PJ, Williams SD, Einhorn LH. Klinefelter's syndrome associated with mediastinal germ cell neoplasms. Journal of Clinical Oncology. 5: 1290-1294. PMID 3040921 DOI: 10.1200/Jco.1987.5.8.1290  1
1986 Pettenati MJ, Haines JL, Higgins RR, Wappner RS, Palmer CG, Weaver DD. Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature. Human Genetics. 74: 143-54. PMID 3770742 DOI: 10.1007/Bf00282078  1
1986 Schwartz S, Palmer CG, Yu PL, Boughman JA, Cohen MM. Analysis of translocations observed in three different populations. II. Robertsonian translocations. Cytogenetics and Cell Genetics. 42: 53-6. PMID 3720358 DOI: 10.1159/000132250  1
1986 Schwartz S, Palmer CG, Yu PL, Boughman JA, Cohen MM. Analysis of translocations observed in three different populations. I. Reciprocal translocations. Cytogenetics and Cell Genetics. 42: 42-52. PMID 3720357 DOI: 10.1159/000132249  1
1985 Mamula PW, Heerema NA, Palmer CG, Lyons KM, Karn RC. Localization of the human salivary protein complex (SPC) to chromosome band 12p13.2 Cytogenetics and Cell Genetics. 39: 279-284. PMID 4053693 DOI: 10.1159/000132158  1
1985 Heerema NA, Palmer CG, Baehner RL. Karyotypic and clinical findings in a consecutive series of children with acute lymphocytic leukemia. Cancer Genetics and Cytogenetics. 17: 165-79. PMID 3857967 DOI: 10.1016/0165-4608(85)90027-5  1
1984 Young RS, Weaver DD, Kukolich MK, Heerema NA, Palmer CG, Kawira EL, Bender HA. Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new cases. American Journal of Medical Genetics. 17: 437-50. PMID 6199974 DOI: 10.1002/ajmg.1320170207  1
1983 Schwartz S, Palmer CG, Weaver DD, Priest J. Dicentric chromosome 13 and centromere inactivation Human Genetics. 63: 332-337. PMID 6862437 DOI: 10.1007/Bf00274757  1
1983 Young RS, Bader P, Palmer CG. Two children with de novo del(9p) American Journal of Medical Genetics. 14: 751-757. PMID 6846405 DOI: 10.1002/Ajmg.1320140416  1
1983 Palmer CG, Provisor AJ, Weaver DD, Hodes ME, Heerema N. Juvenile chronic granulocytic leukemia in a patient with trisomy 8, neurofibromatosis, and prolonged Epstein-Barr virus infection The Journal of Pediatrics. 102: 888-892. PMID 6304274 DOI: 10.1016/S0022-3476(83)80020-1  1
1982 Butler MG, Russell LJ, Palmer CG, Bull M, Hodes ME. Brief clinical report: a child with radius aplasia, cleft of lip and palate, microcephaly, and unusual chromosome findings. American Journal of Medical Genetics. 13: 369-72. PMID 6961772 DOI: 10.1002/Ajmg.1320130404  1
1982 Keitges EA, Palmer CG, Weaver DD. Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle function Human Genetics. 62: 210-213. PMID 6892018 DOI: 10.1007/Bf00333520  1
1981 Al-Nassar KE, Palmer CG, Conneally PM, Yu PL. The genetic structure of the kuwaiti population II: The distribution of Q-band chromosomal heteromorphisms Human Genetics. 57: 423-427. PMID 7286984 DOI: 10.1007/Bf00281697  1
1981 Al-Nassar KE, Conneally PM, Palmer CG, Yu Pl. The genetic structure of the Kuwaiti population - I. Distribution of 17 markers with genetic distance analysis Human Genetics. 57: 192-198. PMID 7228033 DOI: 10.1007/Bf00282021  1
1981 Lazarus KH, Heerema NA, Palmer CG, Baehner RL. The myeloproliferative reaction in a child with Down syndrome: cytological and chromosomal evidence for a transient leukemia. American Journal of Hematology. 11: 417-23. PMID 6460436 DOI: 10.1002/ajh.2830110411  1
1979 Therman E, Sarto GE, Palmer CG, Kallio H, Denniston C. Position of the human X inactivation center on Xq. Human Genetics. 50: 59-64. PMID 468261 DOI: 10.1007/Bf00295590  1
1978 Morris SM, Palmer CG, Fry FJ, Johnson LK. Effect of ultrasound on human leucocytes sister chromatid exchange analysis Ultrasound in Medicine and Biology. 4: 253-258. PMID 751305 DOI: 10.1016/0301-5629(78)90055-8  1
1976 Khairi S, Palmer CG, Thompson J, Armstrong R. Prenatal diagnosis of fetal abnormality by amniocentesis. The Journal of the Indiana State Medical Association. 69: 623-8. PMID 965771  0.01
1975 Rhine SA, Cain JL, Cleary RE, Palmer CG, Thompson JF. Prenatal sex detection with endocervical smears: successful results utilizing Y-bodyfluoroscence. American Journal of Obstetrics and Gynecology. 122: 155-60. PMID 50740 DOI: 10.1016/S0002-9378(16)33486-X  1
1973 Stafford TM, Palmer CG, Cleary RE. Gonadal dysgenesis with isochromosome X and menstruation American Journal of Obstetrics and Gynecology. 116: 886. PMID 4715948 DOI: 10.1016/0002-9378(73)91031-4  1
1963 HODES ME, PALMER CG, BEATY LE, SWENSON MK, HUBBARD JD. Infectivity experiments with nucleic acids of the Shope rabbit papilloma and derived carcinomas. Journal of the National Cancer Institute. 30: 1-15. PMID 13963766 DOI: 10.1093/Jnci/30.1.1  1
1961 Palmer CG, Hodes ME, Warren AK. The action of synthetic surfactants on membranes of tumor cells. I. Morphological observations Experimental Cell Research. 24: 429-439. PMID 14483392 DOI: 10.1016/0014-4827(61)90444-X  1
1960 Hodes ME, Warren AK, Palmer CG. Inhibition of ehrlich ascites tumour growth by surface-active agents Nature. 188: 157-158. PMID 13714825 DOI: 10.1038/188157A0  1
1958 Hodes ME, Palmer CG, Williams DS. Possible use of synthetic surface-active agents for the preparation of tumour cell nuclei Nature. 182: 529-530. PMID 13577902 DOI: 10.1038/182529A0  1
Show low-probability matches.