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8. A de novo translocation t(6q+; 15q-) in a boy with trisomy 21. Iinuma K; Nakagome Y; Higurashi M Jinrui Idengaku Zasshi; 1975 Sep; 20(2):147-51. PubMed ID: 1238781 [No Abstract] [Full Text] [Related]
9. [Robertsonian translocation 13-22 in the father of a child with free trisomy 21]. Walbaum R; Deroubaix P; Van de Velde MF Pediatrie; 1976; 31(7):697-701. PubMed ID: 1012854 [No Abstract] [Full Text] [Related]
10. [Trisomy 9p. A case of translocation t(9;22) (p11;p11)mat in a little girl]. Genest P; Roussy J; Genest FB; Dumas L Union Med Can; 1977 Jul; 106(7):956-9. PubMed ID: 898406 [No Abstract] [Full Text] [Related]
11. [Trisomy 10p as a result of familial 10/22 translocation]. Zergollern L; Begovic D; Muzinić D Acta Med Iugosl; 1980; 34(2):113-22. PubMed ID: 7405617 [No Abstract] [Full Text] [Related]
12. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation]. Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734 [No Abstract] [Full Text] [Related]
13. Transmission of a t(13q22q) chromosome observed in three generations with segregation of the translocation D1-trisomy syndrome. Abe T; Morita M; Kawai K; Misawa S; Kanai H; Hirose G; Fujita H Humangenetik; 1975 Sep; 30(3):207-15. PubMed ID: 1184006 [TBL] [Abstract][Full Text] [Related]
14. [Identification of 2 familial translocations]. Laurent C; Biemont MC; Robert JM; Dutrillaux B Ann Genet; 1974 Dec; 17(4):279-81. PubMed ID: 4548825 [No Abstract] [Full Text] [Related]
15. 47, XY, t(9pplus;11qplus) in a mlae infant with multiple malformations. Dinno ND; Silvey GL; Weisskopf B Clin Genet; 1974; 6(2):125-31. PubMed ID: 4430152 [No Abstract] [Full Text] [Related]
16. [Trisomy 12(pter----q12) and monosomy 21(pter----q21). A propos of a case]. Arnaud M; Bourrouillou G; Sablayrolles B; Rolland M; Dutau G; Colombies P; Rochiccioli P J Genet Hum; 1984 Dec; 32(5):369-75. PubMed ID: 6527133 [TBL] [Abstract][Full Text] [Related]
17. Partial monosomy 22pter leads to q11 in a newborn with the clinical features of trisomy 13 syndrome. Back E; Stier R; Böhm N; Adlung A; Hameister H Ann Genet; 1980; 23(4):244-8. PubMed ID: 6971606 [TBL] [Abstract][Full Text] [Related]
18. [Trisomy syndrome D (47, XY, D+) in a newborn]. Majlert T; Jaworska M; Stolarska A Pediatr Pol; 1970 Nov; 45(11):1379-82. PubMed ID: 5496174 [No Abstract] [Full Text] [Related]
19. [Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)]. Obry E; Piussan C; Risbourg B; Dutrillaux B Ann Genet; 1980; 23(4):216-20. PubMed ID: 6971599 [TBL] [Abstract][Full Text] [Related]
20. Down's syndrome. I. Cytogenetics. Maximilian C; Duca D; Pop T; Toncescu N; Ioan D Endocrinologie; 1980; 18(4):273-5. PubMed ID: 6451918 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]