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.
3. Familial transmission of a presumptive D/E (13-15/17-18) short arm translocation. Cohen MM, Lockwood MA. Pediatr Res; 1967 Mar; 1(2):104-9. PubMed ID: 6029809 [No Abstract] [Full Text] [Related]
4. Congenital heart disease in an infant with the Smith-Lemli-Opitz syndrome. Park SC, Needles CF, Dimich I, Sussman L. J Pediatr; 1968 Dec; 73(6):896-902. PubMed ID: 4386913 [No Abstract] [Full Text] [Related]
5. [Two malformative syndromes possibly unifiable: Ullrich-Feichtiger and Smith-Lemli-Opitz syndromes. Case report]. Lendvai D, Castello MA, Ballati G. Minerva Pediatr; 1969 Jan 14; 21(2):56-61. PubMed ID: 4388355 [No Abstract] [Full Text] [Related]
7. Adams-Oliver syndrome associated with congenital heart defect: not a coincidence. David A, Rozé JC, Melon-David V. Am J Med Genet; 1991 Jul 01; 40(1):126-7. PubMed ID: 1887843 [No Abstract] [Full Text] [Related]
8. [Congenital heart defects associated with developmental abnormalities of the fingers]. Fonó R. Orv Hetil; 1966 Jun 12; 107(24):1126-9. PubMed ID: 5944848 [No Abstract] [Full Text] [Related]
14. [Postaxial polydactyly in a female neonate associated with hydrocolpos due to vaginal atresia and with a congenital cardiopathy: the McKusick-Kaufman syndrome]. Castel Y, Toudic L, Alix D, Le Guern H, Colin A. J Genet Hum; 1982 Nov 12; 30(4):329-37. PubMed ID: 7169598 [Abstract] [Full Text] [Related]