Loss of function in ROBO1 is associated with tetralogy of Fallot and septal defects
BACKGROUND: Congenital heart disease (CHD) is a common birth defect affecting approximately 1% of newborns. Great progress has been made in elucidating the genetic aetiology of CHD with advances in genomic technology, which we leveraged in recovering a new pathway affecting heart development in huma...
Prif Awduron: | Kruszka, P, Tanpaiboon, P, Neas, K, Crosby, K, Berger, S, Martinez, A, Addissie, Y, Pongprot, Y, Sittiwangkul, R, Silvilairat, S, Makonkawkeyoon, K, Yu, L, Wynn, J, Bennett, J, Mefford, H, Reynolds, W, Liu, X, Mommersteeg, M, Chung, W, Lo, C, Muenke, M |
---|---|
Fformat: | Journal article |
Iaith: | English |
Cyhoeddwyd: |
BMJ Publishing Group
2017
|
Eitemau Tebyg
-
Intermittent′ restrictive ventricular septal defect in Tetralogy of Fallot
gan: Sudhir S Shetkar, et al.
Cyhoeddwyd: (2015-01-01) -
Pheochromocytoma presenting with QT prolongation and catecholamine-induced myocarditis in a child
gan: Kwannapas Saengsin, et al.
Cyhoeddwyd: (2023-01-01) -
80. Atrioventricular septal defect and tetralogy of Fallot: A 16-year experience
gan: S. Al-Ahdal, et al.
Cyhoeddwyd: (2015-10-01) -
Prenatal diagnosis of tetralogy of Fallot with a restrictive ventricular septal defect
gan: Villalaín, Cecilia, et al.
Cyhoeddwyd: (2021-02-01) -
Tetralogy of Fallot
gan: Anderson Robert H, et al.
Cyhoeddwyd: (2009-01-01)