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Autor:
Mirna Toledo-Bahena, Alan D. Irvine, Nnenna G. Agim, Richard C. Wang, Donald A. Glass, Irene Dougherty, Mohammed Kanchwala, Chao Xing, Monique G. Kumar, An Tran, Marwan Shinawi, David R. Berk, Andrea Tovar-Garza, Jonathan J. Rios, Christy Purnadi, Tommy Hyatt
Publikováno v:
Human mutationREFERENCES. 42(8)
CDAGS Syndrome is a rare congenital disorder characterized by Craniosynostosis, Delayed closure of the fontanelles, cranial defects, clavicular hypoplasia, Anal and Genitourinary malformations, and Skin manifestations. We performed whole exome and Sa