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.
114 related articles for article (PubMed ID: 8230166)
1. Sex linked valvular dysplasia. Newbury-Ecob RA; Zuccollo JM; Rutter N; Young ID J Med Genet; 1993 Oct; 30(10):873-4. PubMed ID: 8230166 [TBL] [Abstract][Full Text] [Related]
2. X-linked recessive inheritance of an orofaciodigital syndrome with partial expression in females and survival of affected males. Edwards M; Mulcahy D; Turner G Clin Genet; 1988 Nov; 34(5):325-32. PubMed ID: 3229001 [TBL] [Abstract][Full Text] [Related]
3. X-linked laterality sequence: situs inversus, complex cardiac defects, splenic defects. Mathias RS; Lacro RV; Jones KL Am J Med Genet; 1987 Sep; 28(1):111-6. PubMed ID: 3674105 [TBL] [Abstract][Full Text] [Related]
4. A new X-linked dysplasia gigantism syndrome: identical with the Simpson dysplasia syndrome? Behmel A; Plöchl E; Rosenkranz W Hum Genet; 1984; 67(4):409-13. PubMed ID: 6490008 [TBL] [Abstract][Full Text] [Related]
5. Mutations in VEGFA are associated with congenital left ventricular outflow tract obstruction. Zhao W; Wang J; Shen J; Sun K; Zhu J; Yu T; Ji W; Chen Y; Fu Q; Li F Biochem Biophys Res Commun; 2010 May; 396(2):483-8. PubMed ID: 20420808 [TBL] [Abstract][Full Text] [Related]
6. Association of common variants in ERBB4 with congenital left ventricular outflow tract obstruction defects. McBride KL; Zender GA; Fitzgerald-Butt SM; Seagraves NJ; Fernbach SD; Zapata G; Lewin M; Towbin JA; Belmont JW Birth Defects Res A Clin Mol Teratol; 2011 Mar; 91(3):162-8. PubMed ID: 21290564 [TBL] [Abstract][Full Text] [Related]
7. Design and rationale of a genetic cohort study on congenital cardiac disease: experiences from a multi-institutional platform in Quebec. Dubé MP; Bigras JL; Thibeault M; Bureau N; Chetaille P; Richter A; Mercier J; Bellavance M; Rohlicek C; Rozen R; Nemer M; Khairy P; Gendron R; Andelfinger G Cardiol Young; 2011 Dec; 21(6):654-64. PubMed ID: 21729494 [TBL] [Abstract][Full Text] [Related]
8. A family showing apparent X linked inheritance of both anencephaly and spina bifida. Jensson O; Arnason A; Gunnarsdottir H; Petursdottir I; Fossdal R; Hreidarsson S J Med Genet; 1988 Apr; 25(4):227-9. PubMed ID: 3285008 [TBL] [Abstract][Full Text] [Related]
10. Three distinct types of X-linked arthrogryposis seen in 6 families. Hall JG; Reed SD; Scott CI; Rogers JG; Jones KL; Camarano A Clin Genet; 1982 Feb; 21(2):81-97. PubMed ID: 7200838 [TBL] [Abstract][Full Text] [Related]
19. VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance. Wang H; Hunter AG; Clifford B; McLaughlin M; Thompson D Am J Med Genet; 1993 Aug; 47(1):114-7. PubMed ID: 8368240 [TBL] [Abstract][Full Text] [Related]
20. [Genetics of congenital cardiopathies]. Moreno García M; Gómez Rodríguez MJ; Barreiro Miranda E An Esp Pediatr; 2000 Jul; 53(1):30-9. PubMed ID: 10998401 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]