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.
72 related articles for article (PubMed ID: 668753)
41. [Ostium atrioventricularis communis; case of 10 year old child; postmortem study]. GARCIA O Rev Cubana Pediatr; 1950 Aug; 22(8):451-67. PubMed ID: 14776270 [No Abstract] [Full Text] [Related]
42. Rare and Common Variants Uncover the Role of the Atria in Coarctation of the Aorta. Zhu W; Williams K; Young C; Lin JH; Teekakirikul P; Lo CW Genes (Basel); 2022 Apr; 13(4):. PubMed ID: 35456442 [TBL] [Abstract][Full Text] [Related]
43. Genetic Etiology of Left-Sided Obstructive Heart Lesions: A Story in Development. Parker LE; Landstrom AP J Am Heart Assoc; 2021 Jan; 10(2):e019006. PubMed ID: 33432820 [TBL] [Abstract][Full Text] [Related]
44. Some Isolated Cardiac Malformations Can Be Related to Laterality Defects. Versacci P; Pugnaloni F; Digilio MC; Putotto C; Unolt M; Calcagni G; Baban A; Marino B J Cardiovasc Dev Dis; 2018 May; 5(2):. PubMed ID: 29724030 [TBL] [Abstract][Full Text] [Related]
45. Familial recurrence of congenital heart disease: an overview and review of the literature. Calcagni G; Digilio MC; Sarkozy A; Dallapiccola B; Marino B Eur J Pediatr; 2007 Feb; 166(2):111-6. PubMed ID: 17091259 [TBL] [Abstract][Full Text] [Related]
46. Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion. Digilio MC; Marino B; Giannotti A; Toscano A; Dallapiccola B J Med Genet; 1997 Mar; 34(3):188-90. PubMed ID: 9132487 [TBL] [Abstract][Full Text] [Related]
47. A single major-gene defect underlying cardiac conotruncal malformations interferes with myocardial growth during embryonic development: studies in the CTD line of keeshond dogs. Patterson DF; Pexieder T; Schnarr WR; Navratil T; Alaili R Am J Hum Genet; 1993 Feb; 52(2):388-97. PubMed ID: 8430699 [TBL] [Abstract][Full Text] [Related]
48. Familial atrioventricular septal defect: possible genetic mechanisms. Kumar A; Williams CA; Victorica BE Br Heart J; 1994 Jan; 71(1):79-81. PubMed ID: 8297702 [TBL] [Abstract][Full Text] [Related]
49. A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21. Wilson L; Curtis A; Korenberg JR; Schipper RD; Allan L; Chenevix-Trench G; Stephenson A; Goodship J; Burn J Am J Hum Genet; 1993 Dec; 53(6):1262-8. PubMed ID: 8250042 [TBL] [Abstract][Full Text] [Related]
50. Genetic study of congenital heart defects in Northern Ireland (1974-1978). Hanna EJ; Nevin NC; Nelson J J Med Genet; 1994 Nov; 31(11):858-63. PubMed ID: 7853370 [TBL] [Abstract][Full Text] [Related]