Familial Ebstein's anomaly.

Author:

Rosenmann A,Arad I,Simcha A,Schaap T

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference19 articles.

1. Familial Ebstein's anomaly of the tricuspid valve;Donegan, Jr., C.C.; Moore, M.M.; Wiley, Jr., T.M.; Hernandez, F.A.; Green, Jr., J.R.; Schiebler, G.L.;American Heart Journal,1968

2. Genetics and congenital heart disease;Emanuel, R.;British Heart Journal,1970

3. Congenital heart disease in sibships ascertained by two affected siblings;Fuhrman, W.;Humangenetik,1968

4. Normal und Pathologische Entwickling des Menschlinchen Herzens;Goerttler, K.,1958

5. Maladie d'Ebstein dans une meme fratrie;Gouffault, J.; Le Damany, L.;Archives des Maladies du Coeur et des Vaisseaux,1956

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1. Rare loss-of-function variants in matrisome genes are enriched in Ebstein’s anomaly;Human Genetics and Genomics Advances;2024-01

2. Heterozygous nonsense variants in laminin subunit 3α resulting in Ebstein’s anomaly;Human Genetics and Genomics Advances;2023-10

3. Ebstein’s Anomaly;JACC: Clinical Electrophysiology;2021-09

4. Ebstein Anomaly: Assessment, Management, and Timing of Intervention;Current Treatment Options in Cardiovascular Medicine;2014-08-22

5. Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutation;American Journal of Medical Genetics Part A;2013-08-16

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