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Journal Abstract Search
163 related items for PubMed ID: 4243780
1. [A study of the offspring of t(21q Dq) translocation carriers]. Dutrillaux B, Lejeune J. Ann Genet; 1969 Jun; 12(2):77-82. PubMed ID: 4243780 [No Abstract] [Full Text] [Related]
2. [Familial occurrence of translocation (13q 14q) and 14q 21q)]. Czerski P, Rogóyski A, Stolarska A. Pediatr Pol; 1977 Apr; 52(4):429-35. PubMed ID: 141033 [No Abstract] [Full Text] [Related]
4. Down's syndrome associated with a familial (21q-; 22q+) translocation. Cohen MM, Davidson RG. Cytogenetics; 1967 Apr; 6(5):321-30. PubMed ID: 4231490 [No Abstract] [Full Text] [Related]
5. [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]
6. Familial (13q14q) and (14q21q) translocation. Czerski P, Rogóyski A, Stolarska A, Wróblewska K. Helv Paediatr Acta; 1974 Nov; 29(5):443-6. PubMed ID: 4281417 [No Abstract] [Full Text] [Related]
7. [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]
8. Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the Down syndrome. Kitsiou-Tzeli S, Hallett JJ, Atkins L, Latt SA, Holmes LB. Am J Med Genet; 1984 Aug; 18(4):725-9. PubMed ID: 6237580 [Abstract] [Full Text] [Related]
9. A peculiar t(21 ; 14) translocation, associated with a pericentric inversion of the Y chromosome in a mongol boy. Orye E, Verhaaren H. Ann Genet; 1974 Sep; 17(3):217-20. PubMed ID: 4141590 [No Abstract] [Full Text] [Related]
10. Report of large kinship with familial translocation between chromosomes 21 and 22. Brissenden JE, Costa MT, Roberts MH. Can Med Assoc J; 1977 Dec 17; 117(12):1411-3. PubMed ID: 145313 [Abstract] [Full Text] [Related]
11. [T (14q-; 21q + ) translocation in the father. Partial trisomy 14 and monosomy 21 in the daughter]. Laurent C, Dutrillaux B, Biemont MC, Genoud J, Bethenod M. Ann Genet; 1973 Dec 17; 16(4):281-4. PubMed ID: 4544094 [No Abstract] [Full Text] [Related]
12. [Functional analysis of chromosome translocation (DqGq) in hereditary Down's syndrome by DNA replication pattern]. Abe T. Saishin Igaku; 1968 Feb 10; 24(2):313-6. PubMed ID: 4239275 [No Abstract] [Full Text] [Related]
13. [Translocation mongolism (presentation of a family with 14/21 translocation)]. Sorge G, Garozzo R, Mollica F. Pediatria (Napoli); 1977 Sep 30; 85(3):465-73. PubMed ID: 145579 [No Abstract] [Full Text] [Related]
14. [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 Sep 30; 18(3):223-8. PubMed ID: 6235655 [Abstract] [Full Text] [Related]
15. Familial Down's syndrome with G-G translocation. Hubner H, Jeske J, Dzida J. Pol Med Sci Hist Bull; 1969 Oct 30; 12(4):164-7. PubMed ID: 4257690 [No Abstract] [Full Text] [Related]
16. Down syndrome associated with a familial 14/21 translocation. Hanna EJ, Johnston WP, Nevin NC. Ulster Med J; 1981 Oct 30; 50(2):95-8. PubMed ID: 6460372 [No Abstract] [Full Text] [Related]
17. Trisomy and D/G translocation mongolism in brothers. Ingalls TH, Henry TA. N Engl J Med; 1968 Jan 04; 278(1):10-4. PubMed ID: 4229204 [No Abstract] [Full Text] [Related]
18. Structural variation in human nitotic chromosomes. Leisti J. Ann Acad Sci Fenn Biol; 1971 Jan 04; 179():1-69. PubMed ID: 4261167 [No Abstract] [Full Text] [Related]
20. [Significance of chromosome translocations from the G-D group in the karyotype of the mother of 2 children with Down's syndrome]. Dobrzańska A, Kostrzewski J. Pediatr Pol; 1970 Feb 04; 45(2):211-5. PubMed ID: 4245096 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]