Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 Deletions
Tiong Yang Tan(Royal Children's Hospital), Peter G. Farlie(Royal Children's Hospital), Erik G. Puffenberger(Clinic for Special Children), Fanny Pelluard(Université de Bordeaux), Tobias B. Haack(Technical University of Munich), Peter Simm(The University of Sydney), Karlla W. Brigatti(Clinic for Special Children), Gwenaël Le Guyader(Université de Poitiers), Ron A. Deckelbaum(Regeneron (United States)), Kevin A. Strauss(Clinic for Special Children), John D. Overton(Yale University), Virginia C. Hughes(Regeneron (United States)), Katharina Steindl(University of Zurich), Anita Rauch(Friedrich-Alexander-Universität Erlangen-Nürnberg), Susannah Brydges(Regeneron (United States)), Stefanie Eggers(The University of Sydney), Ioanna Skubas(Regeneron (United States)), Michael Hofbeck(University Children's Hospital Tübingen), Melissa G. Dominguez(Regeneron (United States)), Pascal Joset(University of Zurich), Stephan Waldmueller(Zentrum für Kinderheilkunde), Claudia Gonzaga‐Jauregui(Duke University), Nanditha Das(Regeneron (United States)), Marc Sturm(University of Tübingen), Håkon Håkonarson(Children's Hospital of Philadelphia), Sarah Hatsell(Regeneron (United States)), Elizabeth Bhoj(Children's Hospital of Philadelphia), Chia-Jen Siao(Regeneron (United States)), Dong Li(Children's Hospital of Philadelphia), Bryn Jones(Murdoch Children's Research Institute), Liqin Xie(Regeneron (United States)), Valerie Mayne(Royal Children's Hospital), Aris N. Economides(Regeneron (United States)), Naomi L. Baker(The University of Melbourne), Angelika Rieß(University of Tübingen)
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