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2. Familial translocation t(3p-;21q+) associated with both Down's and Sturge-Weber's syndrome in unbalanced state. Habedank M; Kampe G Humangenetik; 1975 Sep; 29(3):207-16. PubMed ID: 126210 [TBL] [Abstract][Full Text] [Related]
3. Mosaic Down's syndrome with de novo 45,XX,-21,-22,+t(21q;22q)/46,XX,-21,+t(21q;21q) rearrangement. Tharapel AT; Redheendran R; Mankinen CB; Kukolich MK J Med Genet; 1984 Oct; 21(5):391-5. PubMed ID: 6239037 [TBL] [Abstract][Full Text] [Related]
4. A boy with trisomic Down's syndrome and a familial 5-?7 translocation, 47,XY,+21, t (5q-; ?7p+). Yanagisawa S Jinrui Idengaku Zasshi; 1972 Sep; 17(1):38-43. PubMed ID: 4265909 [No Abstract] [Full Text] [Related]
6. Trisomy 9p and unusual translocation mongolism in siblings due to different 3:1 segregations of maternal translocation rcp(9;21)(p11;q11). Habedank M; Faust J Hum Genet; 1978 Jun; 42(3):251-6. PubMed ID: 149755 [TBL] [Abstract][Full Text] [Related]
8. [Sporadic Down's syndrome with isochromosome or translocation 21q/21q (author's transl)]. Moreira LM; Ferrari I Rev Bras Pesqui Med Biol; 1976 Sep; 9(4):193-8. PubMed ID: 136014 [TBL] [Abstract][Full Text] [Related]
9. Unstable telocentric chromosome produced after centric misdivision of a 21q/21q translocated element. Guanti G; Maritato F Hum Genet; 1978 Dec; 45(3):355-62. PubMed ID: 153887 [TBL] [Abstract][Full Text] [Related]
10. Reciprocal translocation, 4q-; 21p+, giving rise to Down's syndrome. Jenkins MB; Boyd L J Med Genet; 1976 Aug; 13(4):323-6. PubMed ID: 134161 [TBL] [Abstract][Full Text] [Related]
11. Probable reciprocal translocation in somatic cells from patients with Down's syndrome. Sonta S; Oishi H Jinrui Idengaku Zasshi; 1974 Sep; 19(2):169-73. PubMed ID: 4280457 [No Abstract] [Full Text] [Related]
12. Translocation and trisomic Down's syndrome in a family with a familial D-G translocation. Zizka J Cytologia (Tokyo); 1969 Sep; 34(3):423-8. PubMed ID: 4244707 [No Abstract] [Full Text] [Related]
13. [Significance of the type of chromosome aberrations and biochemical disorders for diagnosis of Down's syndrome and the phenotype of partial trisomy 21]. Mikiel-Kostyra K; Czerski P; Bartosz G; Sito A; Leyka W Pediatr Pol; 1980 Jan; 55(1):23-32. PubMed ID: 6445053 [No Abstract] [Full Text] [Related]
14. A rare translocation (47,XY,t(2p-;21q+),21+) associated with Down's syndrome. Miller JR; Dill FJ; Corey MJ; Rigg JM J Med Genet; 1970 Dec; 7(4):389-93. PubMed ID: 4250981 [No Abstract] [Full Text] [Related]
15. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)]. Butomo IV; Prozorova MV; Khitrikova LE Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655 [TBL] [Abstract][Full Text] [Related]
16. Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q). Vianna-Morgante AM; Nunesmaia HG J Med Genet; 1978 Aug; 15(4):305-10. PubMed ID: 152355 [TBL] [Abstract][Full Text] [Related]
17. Familial transmission of a (21q22q) translocation. Buckton KE; Newton MS; Lauder IJ; Mey R; Elliot D; Skinner R Cytogenet Cell Genet; 1975; 15(2):103-11. PubMed ID: 126851 [TBL] [Abstract][Full Text] [Related]
18. Partial trisomies of chromosome 21 in man. Two new observations due to translocations 19;21 and 4;21. Pfeiffer RA; Kessel EK; Soer KH Clin Genet; 1977 Mar; 11(3):207-13. PubMed ID: 138497 [TBL] [Abstract][Full Text] [Related]
19. De novo translocation Down's syndrome: risk of recurrence of Down's syndrome. Gardner RJ; Veale AM Clin Genet; 1974; 6(3):160-4. PubMed ID: 4279152 [No Abstract] [Full Text] [Related]