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3. Tertiary trisomy 14q--, due to paternal balanced translocation 46,XY,t(1;14)(q44;q22). Kovacs G; Mihai C Hum Genet; 1979 Jun; 49(2):175-8. PubMed ID: 468247 [TBL] [Abstract][Full Text] [Related]
4. Partial trisomy 13q identified by sequential fluorescence in situ hybridization. Rao VV; Carpenter NJ; Gucsavas M; Coldwell J; Say B Am J Med Genet; 1995 Jul; 58(1):50-3. PubMed ID: 7573156 [TBL] [Abstract][Full Text] [Related]
5. Five familial cases with a trisomy 16p syndrome due to translocation. Leschot NJ; De Nef JJ; Geraedts JP; Becker-Bloemkolk MJ; Talma A; Bijlsma JB; Verjaal M Clin Genet; 1979 Sep; 16(3):205-14. PubMed ID: 487639 [TBL] [Abstract][Full Text] [Related]
6. Partial trisomy 6q, due to balanced maternal translocation (6;22) (q21; p13) or (q21; pter). Stamberg J; Shapiro J; Valle D; Kuhajda FP; Thomas G; Wissow L Clin Genet; 1981 Feb; 19(2):122-5. PubMed ID: 7471508 [TBL] [Abstract][Full Text] [Related]
7. 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; 45(1):89-95. PubMed ID: 730186 [TBL] [Abstract][Full Text] [Related]
8. A case of leprechaunism with chromosome abnormality (46, XX, der(21), t(3;21)(q26 or 27;q22)pat). Iwasaki H; Abe M; Kato H; Shinohara T; Miyata H Jinrui Idengaku Zasshi; 1978 Jun; 23(2):145-51. PubMed ID: 691836 [No Abstract] [Full Text] [Related]
9. 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; 37(4):1230-7. PubMed ID: 19761709 [TBL] [Abstract][Full Text] [Related]
10. Partial trisomy 1 with congenital hydrocephalus and hypogammaglobulinemia: report of one case. Hwu WL; Kuo PL; Hung YT; Chien YH; Chu SY Acta Paediatr Taiwan; 2004; 45(2):97-9. PubMed ID: 15335120 [TBL] [Abstract][Full Text] [Related]
11. Confirmation of proximal 1q duplication using fluorescence in situ hybridization. Chen H; Kusyk CJ; Tuck-Muller CM; Martinez JE; Dorand RD; Wertelecki W Am J Med Genet; 1994 Mar; 50(1):28-31. PubMed ID: 8160749 [TBL] [Abstract][Full Text] [Related]
12. Complete trisomy 1q with mosaic Y;1 translocation: a recurrent aneuploidy presenting diagnostic dilemmas. Scheuerle A; Heller K; Elder F Am J Med Genet A; 2005 Oct; 138A(2):166-70. PubMed ID: 16152651 [TBL] [Abstract][Full Text] [Related]
13. Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy. Kim HJ; Hsu LY; Goldsmith LC; Strauss L; Hirschhorn K J Med Genet; 1977 Apr; 14(2):114-9. PubMed ID: 853317 [TBL] [Abstract][Full Text] [Related]
16. Multiple congenital anomalies in association with supernumerary chromosome 47 inherited from a maternal balanced translocation. Su PH; Chen JY; Hung HM; Chen JP; Wang CM; Chen SJ J Formos Med Assoc; 2002 Apr; 101(4):301-3. PubMed ID: 12101870 [TBL] [Abstract][Full Text] [Related]
17. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation. Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413 [TBL] [Abstract][Full Text] [Related]
18. Partial trisomy of chromosome 3 (3q12 leads to qter) owing to 3q/18p translocation. A trisomy 3q syndrome. Salazar D; Rosenfeld W; Verma RS; Jhaveri RC; Dosik H Am J Dis Child; 1979 Oct; 133(10):1006-8. PubMed ID: 495588 [TBL] [Abstract][Full Text] [Related]
19. Exomphalos and trisomy 18 syndrome. Report of two cases. Zizka J; Balícek P; Pokorná E; Dostalíková K; Kodousková M Hum Genet; 1976 May; 32(2):221-3. PubMed ID: 1270082 [TBL] [Abstract][Full Text] [Related]
20. Trisomy 4q: 46, xy,-11, +der (11), t(4;11) (q27; q25) pat in a child with multiple congenital anomalies. al-Awadi SA; Naguib KK; al-Othman SA; Sundareshan TS Indian J Pediatr; 1988; 55(2):308-11. PubMed ID: 3403028 [No Abstract] [Full Text] [Related] [Next] [New Search]