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11. De novo appearance of a translocation t(5p; 2Iq), and its transmission in both balanced and unbalanced forms to the next generation. Chaganti RS; Morillo-Cucci G; Friis L; Degnan M; German J Ann Genet; 1976 Mar; 19(1):43-8. PubMed ID: 1084121 [TBL] [Abstract][Full Text] [Related]
12. 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 [TBL] [Abstract][Full Text] [Related]
13. Elucidation of the cytogenetic abnormality in a 4p- "phenocopy". Curry CJ; Ying KL; O'Lague P; Tsai J Birth Defects Orig Artic Ser; 1982; 18(3B):275-86. PubMed ID: 7139110 [No 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]
17. [Contribution and considerations on cranio-facial abnormalities caused by chromosomic aberrations in children]. Infortuna M; Gattarello A; Corrado F Pediatr Med Chir; 1984; 6(3):415-23. PubMed ID: 6533589 [TBL] [Abstract][Full Text] [Related]