These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
319 related articles for article (PubMed ID: 4276449)
1. [t(7q-; 21q-plus) and familial and trisomy 21]. Giraud F; Hartung M; Mattei JF; Mattie MG Ann Genet; 1974 Mar; 17(1):49-53. PubMed ID: 4276449 [No Abstract] [Full Text] [Related]
2. [Translocation t(2q-; 21q+) in three generations]. Laurent C; Robert JM Ann Genet; 1968 Mar; 11(1):28-32. PubMed ID: 4233292 [No Abstract] [Full Text] [Related]
3. 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]
4. [Infant with free trisomy 21 and maternal t(14q 22q) translocation]. Forabosco A; Dutrillaux B; Toni G; Lejeune J Ann Genet; 1973 Mar; 16(1):57-9. PubMed ID: 4269148 [No Abstract] [Full Text] [Related]
5. A family with three sibs carrying trisomy 21. Nuzzo F; Stefanini M; Simoni G; Larizza L; Mottura A; Reali E; Franceschini P Ann Genet; 1975 Jun; 18(2):111-6. PubMed ID: 127545 [TBL] [Abstract][Full Text] [Related]
7. [Association of a case of Turner's syndrome with familial t(Cq-; Gp+)]. Laurent C; Bonnet P; Farouz S; Longin B Ann Genet; 1970 Mar; 13(1):61-6. PubMed ID: 5310107 [No Abstract] [Full Text] [Related]
8. [Partial trisomy for the long arm of a C chromosome (?6) through t(Gp+;Cqs+) translocation]. de Grouchy J; Emerit I; Aicardi J Ann Genet; 1969 Jun; 12(2):133-7. PubMed ID: 5308386 [No Abstract] [Full Text] [Related]
9. [Autoradiographic studies of human chromosomes. VII. 5 cases of familial t(DqDq)]. de Grouchy J; Crippa L; German J Ann Genet; 1970 Mar; 13(1):19-37. PubMed ID: 5310103 [No Abstract] [Full Text] [Related]
10. [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]
11. Unusual chromosome aberrations in 3 children with Down syndrome. Osztovics M; Tóth S; Wilhelm O Acta Paediatr Acad Sci Hung; 1982; 23(3):283-9. PubMed ID: 6217717 [TBL] [Abstract][Full Text] [Related]
12. Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution. Hustinx TW; Haar BG; Scheres JM; Rutten FJ Ann Genet; 1974 Dec; 17(4):225-34. PubMed ID: 4281287 [No Abstract] [Full Text] [Related]
13. [Partial C trisomy through translocation t(Cp-;Gp-)]. Deminatti M; Maillard E; Gosselin B; Peltier JM; Bulteel MF; Dupuis C Ann Genet; 1969 Mar; 12(1):36-45. PubMed ID: 5306710 [No Abstract] [Full Text] [Related]
14. 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]
16. Familial Down's syndrome with G-G translocation. Hubner H; Jeske J; Dzida J Pol Med Sci Hist Bull; 1969 Oct; 12(4):164-7. PubMed ID: 4257690 [No Abstract] [Full Text] [Related]
17. An intersexual infant with an extra chromosome. Insley J; Rushton DI; Jones HW Ann Genet; 1968 Jun; 11(2):88-94. PubMed ID: 5303428 [No Abstract] [Full Text] [Related]