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OALib Journal期刊
ISSN: 2333-9721
费用：99美元
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Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans
DOI: 10.1016/j.ajhg.2016.02.016
Anne-Karin Arndt, Anneke？M. Lucassen, Anthony？P. Salmon, Ashok？K. Manickaraj, Barbara Mulder, Bernard Thienpont, Catherine Cosgrove, Catherine？L. Mercer, Chris Thornborough, Christine Harnack, David？I. Wilson, David？R. FitzPatrick, Frances？A. Bu’Lock, G.？Jawahar Swaminathan, Hans-Heiner Kramer, Hashim Abdul-Khaliq, Hugh Watkins, Ita？M. O’Kelly, J.？David Brook, Jacoba Louw, Javier Granados-Riveron, Jeroen Breckpot, Kerry Setchfield, Kirstin Hoff, Koen Devriendt, Lisa？C.A. D’Alessandro, Marc Gewillig, Marc-Phillip Hitz, Matthew？E. Hurles, Okan Toka, Reiner Siebert, Sabine Klaassen, Saeed Al？Turki, Sarah Lindsay, Sebastian？S. Gerety, Seema Mital, Shoumo Bhattacharya, Stephan Schubert, UK10K Consortium
Abstract:
(The American Journal of Human Genetics 94, 574–585; April 3, 2014 Full-Text
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