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12. [Familial balanced chromosome translocation t(12;13) in a family with several deformed stillbirths]. Bommer C; Körner H Zentralbl Gynakol; 1982; 104(24):1578-83. PubMed ID: 6892078 [TBL] [Abstract][Full Text] [Related]
13. Partial trisomy 12p. A newborn child with karyotype 46,XY,der(11), t(11; 12) (q25; p11) mat. Case report and review. Ottolina de Bracamonte N; Velazco JQ; Hammond Figueroa FG Acta Cient Venez; 1982; 33(4):342-7. PubMed ID: 7186725 [No Abstract] [Full Text] [Related]
14. Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature. Taysi K; Chao WT; Monaghan N; Monaco MP Ann Genet; 1983; 26(4):243-6. PubMed ID: 6364954 [TBL] [Abstract][Full Text] [Related]
15. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9. Butler LJ; Eades SM; France NE Ann Genet; 1969 Mar; 12(1):15-27. PubMed ID: 5306708 [No Abstract] [Full Text] [Related]
17. [12 p trisomy. A new case (author's transl)]. Kubryk N; Prieur M; Borde M Ann Pediatr (Paris); 1980 Dec; 27(10):695-9. PubMed ID: 7212558 [No Abstract] [Full Text] [Related]
18. Partial trisomy 9q-in a polymalformed new-born infant. Karyotype: 47,XX, + del (9) (q33). Fryns JP; Smeets E; Eggermont E; Delire C; Van den Berghe H Acta Paediatr Belg; 1978; 31(4):237-40. PubMed ID: 742362 [No Abstract] [Full Text] [Related]
19. Trisomy 18 associated with a familial translocation t(Bq-; 18q+). France NE; Butler LJ Ann Genet; 1969 Mar; 12(1):46-50. PubMed ID: 5306711 [No Abstract] [Full Text] [Related]