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Journal Abstract Search
215 related items for PubMed ID: 7438504
1. Trisomy 18q: 46,XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46,XY,-13,+der(13),t(13;18)(q32;q11). Murthy DS, Patel ZM, Ambani LM. Clin Genet; 1980 Oct; 18(4):233-8. PubMed ID: 7438504 [Abstract] [Full Text] [Related]
5. Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat. Stern LM, Mureh AR. J Med Genet; 1975 Sep; 12(3):305-7. PubMed ID: 1177285 [Abstract] [Full Text] [Related]
8. Partial trisomy 14q due to maternal t(4;14)(p16;q32) in a dysmorphic newborn. Dundar M, Uzak A, Saatci C, Akalin H. Genet Couns; 2011 Sep; 22(3):287-92. PubMed ID: 22029170 [Abstract] [Full Text] [Related]
9. Partial trisomy 13q inherited from balanced translocation (5;13) (p14;q13). Coco R, del Rey G. J Genet Hum; 1978 Dec; 26(4):303-10. PubMed ID: 752064 [Abstract] [Full Text] [Related]
12. Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature. Duckett DP, Roberts SH. Hum Genet; 1981 Dec; 58(4):377-86. PubMed ID: 7035334 [Abstract] [Full Text] [Related]
13. Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation. Hou JW. Chang Gung Med J; 2003 Jan; 26(1):48-52. PubMed ID: 12656309 [Abstract] [Full Text] [Related]
15. Two reciprocal translocations t(9p+;13q-) and t(13q-;21q+): a study of the families. Prieto F, Badia L, Asensi F, Roques V. Hum Genet; 1980 Jan; 54(1):7-11. PubMed ID: 7390483 [Abstract] [Full Text] [Related]