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Journal description
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Details for article 11 of 28 found articles
| Title: |
De Novo Mutations in NALCN Cause a Syndrome Characterized by Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay |
| Author: |
Chong, Jessica X. McMillin, Margaret J. Shively, Kathryn M. Beck, Anita E. Marvin, Colby T. Armenteros, Jose R. Buckingham, Kati J. Nkinsi, Naomi T. Boyle, Evan A. Berry, Margaret N. Bocian, Maureen Foulds, Nicola Uzielli, Maria Luisa Giovannucci Haldeman-Englert, Chad Hennekam, Raoul C.M. Kaplan, Paige Kline, Antonie D. Mercer, Catherine L. Nowaczyk, Malgorzata J.M. Klein Wassink-Ruiter, Jolien S. McPherson, Elizabeth W. Moreno, Regina A. Scheuerle, Angela E. Shashi, Vandana Stevens, Cathy A. Carey, John C. Monteil, Arnaud Lory, Philippe Tabor, Holly K. Smith, Joshua D. Shendure, Jay Nickerson, Deborah A. Bamshad, Michael J. |
| Appeared in: |
The American journal of human genetics |
| Paging: | Volume 96 (2015) nr. 3 pages 12 p. |
| Year: |
2015 |
| Contents: | |
| Publisher: |
The American Society of Human Genetics |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 11 of 28 found articles
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