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4. [Karyotypic study of newborn infants with developmental defects and of premature infants]. Chebotarev AN Pediatriia; 1972 Nov; 51(11):74-5. PubMed ID: 4668246 [No Abstract] [Full Text] [Related]
5. [Pathogenesis of multiple developmental anomalies]. Rozynkowa D Pol Tyg Lek; 1972 Jan; 27(1):1-3. PubMed ID: 5060027 [No Abstract] [Full Text] [Related]
6. Chromosome-10 defects in two newborn infants. Zorn E Hosp Pract (Off Ed); 1984 Dec; 19(12):34I-34J, 34O-34P. PubMed ID: 6438132 [No Abstract] [Full Text] [Related]
8. Familial D-D translocation. A family showing transmission through three generations; a case with multiple congenital malformations, and a case of regular 21-trisomic Down's syndrome. Visfeldt J Acta Pathol Microbiol Scand; 1969; 75(4):545-54. PubMed ID: 4246134 [No Abstract] [Full Text] [Related]
10. [Intrauterine diagnosis of a chromosome translocation]. Aula P; Karjalainen O; Leisti J Duodecim; 1971; 87(20):1372-7. PubMed ID: 5115096 [No Abstract] [Full Text] [Related]
11. [Cumulative developmental anomalies and the incidence of ring-chromosome (C) in one family]. Gács G; Schuler D Orv Hetil; 1969 Aug; 110(32):1852-3. PubMed ID: 5809883 [No Abstract] [Full Text] [Related]
12. [Partial trisomy C through a familial translocation t(Cq+;Cq-)]. Lejeune J; Rethoré MO; Berger R; Abonyi D; Dutrillaux B; See G Ann Genet; 1968 Sep; 11(3):171-5. PubMed ID: 5304617 [No Abstract] [Full Text] [Related]
14. [Genetic studies of married couples with children having developmental defects]. Garsiia-Solano A Akush Ginekol (Mosk); 1976 Dec; (12):20-4. PubMed ID: 1020770 [No Abstract] [Full Text] [Related]
15. DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review. Demczuk S; Aurias A Ann Genet; 1995; 38(2):59-76. PubMed ID: 7486827 [TBL] [Abstract][Full Text] [Related]
16. Congenital defects of the breast - an autosomal dominant trait. Nelson MM; Cooper CK S Afr Med J; 1982 Mar; 61(12):434-6. PubMed ID: 7064019 [TBL] [Abstract][Full Text] [Related]