Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): Confirmation of the Mowat‐Wilson syndrome
- 7 October 2002
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 116A (4), 385-388
- https://doi.org/10.1002/ajmg.a.10855
Abstract
No abstract availableKeywords
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