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4. A balanced translocation t(4;9) (q35;q12) with a breakpoint within the heterochromatic region of chromosome 9 in a woman with recurrent abortion. Neri G; Serra A; Bova R; Natale MT; Tedeschi B Clin Genet; 1980 Oct; 18(4):239-43. PubMed ID: 7438505 [TBL] [Abstract][Full Text] [Related]
5. Ring (13),t(2;6) associated with familial fragile (16). Ventruto V; Rinaldi A; Renda S; Stabile M; Rinaldi MM; Cavaliere ML; Conte N; Aveta V J Med Genet; 1984 Jun; 21(3):233. PubMed ID: 6748026 [No Abstract] [Full Text] [Related]
6. Double balanced chromosomal translocation carrier (6;8), (13;14)--a case report: critique and response. Young RS J Hered; 1984; 75(2):154. PubMed ID: 6715867 [No Abstract] [Full Text] [Related]
7. [A+(8,13) translocation followed for 3 generations]. Turpin JC; Duc JP; Larget-Piet L; Couturier-Turpin MH; Tamboise A Pediatrie; 1981 Sep; 36(6):469-77. PubMed ID: 7312517 [No Abstract] [Full Text] [Related]
8. [Chromosome rearrangements (balanced translocations) and their importance in perinatal pathology]. Khodzhaeva ZS Akush Ginekol (Mosk); 1981 Jan; (1):9-12. PubMed ID: 7013527 [No Abstract] [Full Text] [Related]
9. Balanced rearrangement of chromosomes 2, 5, and 13 in a family with duplication 5q and fetal loss. Evans MI; White BJ; Kent SG; Levine MA; Levin SW; Larsen JW Am J Med Genet; 1984 Dec; 19(4):783-90. PubMed ID: 6517101 [TBL] [Abstract][Full Text] [Related]
10. A new balanced translocation in humans: t(3;8) (q21;q24). Verma RS; Dosik H; Salazar JD J Reprod Med; 1981 Mar; 26(3):133-4. PubMed ID: 7230148 [No Abstract] [Full Text] [Related]
12. [The role of chromosomes in the aetiology of human abortion]. Kotzé GM; Retief AE S Afr Med J; 1978 Sep; 54(14):562-6. PubMed ID: 734601 [TBL] [Abstract][Full Text] [Related]
13. Familial 5/14 translocation with triple X and 47,XY + 14q. Lancet M; Sindel L; Segal I Clin Genet; 1981 Jul; 20(1):40-3. PubMed ID: 7296947 [TBL] [Abstract][Full Text] [Related]
14. Postzygotic D/D translocation homozygosity associated with recurrent abortions. Maeda T; Ohno M; Takada M; Matsunobu A; Arai M Am J Med Genet; 1983 Jul; 15(3):389-92. PubMed ID: 6881208 [TBL] [Abstract][Full Text] [Related]
15. Familial dicentric translocation t(13;18)(p13;p11.2) ascertained by recurrent miscarriages. Daniel A; Perel ID; Clarke AJ; Saville T J Med Genet; 1979 Feb; 16(1):73-5. PubMed ID: 469891 [TBL] [Abstract][Full Text] [Related]
16. Unstable familial translocations: A t(11;22)mat inherited as a t(11;15). Tomkins DJ Am J Hum Genet; 1981 Sep; 33(5):745-51. PubMed ID: 7294023 [TBL] [Abstract][Full Text] [Related]
17. Duplication of part of the long arm of chromosome 8 due to a familial 8;13 translocation. Bredberg A; Iselius L; Lindgren L; Lundmark KM Hereditas; 1982; 96(1):105-8. PubMed ID: 7085335 [No Abstract] [Full Text] [Related]