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Journal Abstract Search
215 related items for PubMed ID: 7438504
21. A Case of a Derivative Chromosome: der(Y)t(Y;18)Pat with Congenital Abnormalities. Huang S, Xia Y, Ding H, Wang Y, Wu Y, Chen S, Zhuang J, Li P. Fetal Pediatr Pathol; 2021 Jun; 40(3):256-261. PubMed ID: 31805817 [Abstract] [Full Text] [Related]
22. Partial monosomy 13q and partial trisomy 18p: case report with necropsy findings. Beneck D, Greco MA, Wolman SR, McMorrow LE, Jansen V, Cason J. J Med Genet; 1986 Jun; 23(3):260-3. PubMed ID: 3723557 [Abstract] [Full Text] [Related]
23. Trisomy 20pter = to q11 in a malformed boy from a t(13;20)(p11;q11) translocation-carrier mother. Schinzel A. Hum Genet; 1980 Feb; 53(2):169-72. PubMed ID: 7358383 [Abstract] [Full Text] [Related]
25. A balanced 13-18 translocation [46,XY,t(13q-;18q+)] in the father of an infant with multiple anomalies. McGilvray E, Kajii T, Freund M, Bamatter F, Klein D. Humangenetik; 1971 Feb; 12(4):316-22. PubMed ID: 5564360 [No Abstract] [Full Text] [Related]
26. Trisomy 4p and deletion 4p- in a family having translocation, t(4p-; 12p+). Mortimer JG, Chewings W, Miethke P, Smith GF. Hum Hered; 1978 Feb; 28(2):132-40. PubMed ID: 621087 [Abstract] [Full Text] [Related]
27. Partial trisomy 18q in a newborn with typical 18 trisomy phenotype. Fryns JP, Detavernier F, van Fleteren A, van den Berghe H. Hum Genet; 1978 Oct 31; 44(2):201-5. PubMed ID: 730164 [Abstract] [Full Text] [Related]
28. Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22. Dawson AJ, Mears AJ, Chudley AE, Bech-Hansen T, McDermid H. J Med Genet; 1996 Nov 31; 33(11):952-6. PubMed ID: 8950677 [Abstract] [Full Text] [Related]
29. Partial trisomies 13 and 22 due to nondisjunction of a maternal reciprocal translocation, t(13;22)(q22;q11). Mutchinick O, Ruz L, Jiménez R. Hum Genet; 1978 Nov 24; 45(1):89-95. PubMed ID: 730186 [Abstract] [Full Text] [Related]
30. Trisomy 14 mosaicism with t(14;15)(q11;p11) in offspring of a balanced translocation carrier mother. Fujimoto A, Lin MS, Korula SR, Wilson MG. Am J Med Genet; 1985 Oct 24; 22(2):333-42. PubMed ID: 4050866 [Abstract] [Full Text] [Related]
31. Partial distal trisomy 13q resulting from familial reciprocal 5/13 translocation. Yanagisawa S, Yokoyama H, Agena N. Hum Genet; 1978 Dec 29; 45(3):345-50. PubMed ID: 738734 [Abstract] [Full Text] [Related]
32. Partial monosomy 10q and partial trisomy 9q with anal atresia due to maternal translocation: t(9;10)(q32;q26). Tsukuda T, Nagata I, Sawada H, Murakami J, Hanaki K, Urashima H, Kaneda T, Shimizu N, Kaibara N, Kodama N, Ohzeki T, Shiraki K. Clin Genet; 1996 Oct 29; 50(4):220-2. PubMed ID: 9001803 [Abstract] [Full Text] [Related]
33. 'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations. Brimblecombe FS, Lewis FJ, Vowles M. J Med Genet; 1977 Aug 29; 14(4):271-4. PubMed ID: 926139 [Abstract] [Full Text] [Related]
36. Tertiary trisomy 14q--, due to paternal balanced translocation 46,XY,t(1;14)(q44;q22). Kovacs G, Mihai C. Hum Genet; 1979 Jun 19; 49(2):175-8. PubMed ID: 468247 [Abstract] [Full Text] [Related]
37. Partial trisomy for the short arm of chromosome 2 due to familial balance translocation. Sekhon GS, Taysi K, Rath R. Hum Genet; 1978 Oct 19; 44(1):99-103. PubMed ID: 711241 [Abstract] [Full Text] [Related]
38. Partial trisomy for the long arm of chromosome 7 due to familial balanced translocation. Schmid M, Wolf J, Nestler H, Krone W. Hum Genet; 1979 Jul 18; 49(3):283-9. PubMed ID: 478537 [Abstract] [Full Text] [Related]
39. Distal trisomy of 10q with distal monosomy of 15q due to a paternal translocation. Sun SC, Luo FW, Song HW, He JB, Peng YS. J Int Med Res; 2009 Jul 18; 37(4):1230-7. PubMed ID: 19761709 [Abstract] [Full Text] [Related]