Familial ventricular aneurysms and septal defects map to chromosome 10p15-Reference-Cited by-同舟云学术

Familial ventricular aneurysms and septal defects map to chromosome 10p15

Published:2010-12-18 Issue:5 Volume:32 Page:568-573
ISSN:0195-668X
Container-title:European Heart Journal
language:en
Short-container-title:

Author:

Tremblay Nicolas,Yang Shi Wei,Hitz Marc-Phillip,Asselin Géraldine,Ginns Jonathan,Riopel Kathleen,Gendron Roxanne,Montpetit Alexandre,Duhig Edwina,Dubé Marie-Pierre,Radford Dorothy,Andelfinger Gregor

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

Link

http://academic.oup.com/eurheartj/article-pdf/32/5/568/17049670/ehq447.pdf

Reference33 articles.

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2. Genetic factors in congenital heart malformation;Clin Genet,2008

3. Familial recurrence of congenital heart disease in patients with ostium secundum atrial septal defect;Eur Heart J,2005

4. Mutation in myosin heavy chain 6 causes atrial septal defect;Nat Genet,2005

5. NKX2.5 mutations in patients with congenital heart disease;J Am Coll Cardiol,2003

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4. Case Report: Clinical Description of a Patient Carrying a 12.48 Mb Microdeletion Involving the 10p13–15.3 Region;Frontiers in Pediatrics;2021-02-25

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