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Birth defects

X-Linked Genes and Risk of Orofacial Clefts: Evidence from Two Population-Based Studies in Scandinavia

Astanand Jugessur, Øivind Skare, [ ... ], Håkon K. Gjessing

Deficient Signaling via Alk2 (Acvr1) Leads to Bicuspid Aortic Valve Development

Penny S. Thomas, Somyoth Sridurongrit, Pilar Ruiz-Lozano, Vesa Kaartinen

Propylthiouracil Is Teratogenic in Murine Embryos

Valeria C. Benavides, Murali K. Mallela, [ ... ], Scott A. Rivkees

Effect of the G375C and G346E Achondroplasia Mutations on FGFR3 Activation

Lijuan He, Christopher Serrano, [ ... ], Kalina Hristova

BMP4 Was Associated with NSCL/P in an Asian Population

Qianqian Chen, Hong Wang, [ ... ], Terri H. Beaty

Screening of MAMLD1 Mutations in 70 Children with 46,XY DSD: Identification and Functional Analysis of Two New Mutations

Nicolas Kalfa, Maki Fukami, [ ... ], Charles Sultan

Exploring the Caffeine-Induced Teratogenicity on Neurodevelopment Using Early Chick Embryo

Zheng-lai Ma, Yang Qin, [ ... ], Xuesong Yang

Asymmetrical Dimethylarginine - More Sensitive than NT-proBNP to Diagnose Heart Failure in Adults with Congenital Heart Disease

Oktay Tutarel, Agnieszka Denecke, [ ... ], Jan T. Kielstein

Genetic Polymorphisms of the TYMS Gene Are Not Associated with Congenital Cardiac Septal Defects in a Han Chinese Population

Jian-Yuan Zhao, Jing-Wei Sun, [ ... ], Hong-Yan Wang

Healthy Growth in Children with Down Syndrome

Helma B. M. Van Gameren-Oosterom, Paula Van Dommelen, [ ... ], Jacobus P. Van Wouwe

Conditional Ablation of Ezh2 in Murine Hearts Reveals Its Essential Roles in Endocardial Cushion Formation, Cardiomyocyte Proliferation and Survival

Li Chen, Yanlin Ma, [ ... ], Jun Wang

Genetic Mapping and Exome Sequencing Identify Variants Associated with Five Novel Diseases

Erik G. Puffenberger, Robert N. Jinks, [ ... ], Kevin A. Strauss

Cardiac Alpha-Myosin (MYH6) Is the Predominant Sarcomeric Disease Gene for Familial Atrial Septal Defects

Maximilian G. Posch, Stephan Waldmuller, [ ... ], Cemil Özcelik

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