A systematic variant screening in familial cases of congenital heart defects demonstrates the usefulness of molecular genetics in this field-Reference-Cited by-同舟云学术

A systematic variant screening in familial cases of congenital heart defects demonstrates the usefulness of molecular genetics in this field

Published:2015-05-27 Issue:2 Volume:24 Page:228-236
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

El Malti Rajae,Liu Hui,Doray Bérénice,Thauvin Christel,Maltret Alice,Dauphin Claire,Gonçalves-Rocha Miguel,Teboul Michel,Blanchet Patricia,Roume Joëlle,Gronier Céline,Ducreux Corinne,Veyrier Magali,Marçon François,Acar Philippe,Lusson Jean-René,Levy Marilyne,Beyler Constance,Vigneron Jacqueline,Cordier-Alex Marie-Pierre,Heitz François,Sanlaville Damien,Bonnet Damien,Bouvagnet Patrice

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2015105.pdf

Reference23 articles.

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2. Pradat P, Francannet C, Harris JA, Robert E : The epidemiology of cardiovascular defects, part I: a study based on data from three large registries of congenital malformations. Pediatr Cardiol 2003; 24: 195–221.

3. Andersen TA, Troelsen Kde L, Larsen LA : Of mice and men: molecular genetics of congenital heart disease. Cell Mol Life Sci 2014; 71: 1327–1352.

4. Fahed AC, Gelb BD, Seidman JG, Seidman CE : Genetics of congenital heart disease: the glass half empty. Circ Res 2013; 112: 707–720.

5. Oyen N, Poulsen G, Boyd HA, Wohlfahrt J, Jensen PK, Melbye M : Recurrence of congenital heart defects in families. Circulation 2009; 120: 295–301.

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