Mowat-Wilson syndrome with craniosynostosis: A case report
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32075/fullpdf
Reference9 articles.
1. Clinical features and management issues in Mowat–Wilson syndrome
2. ZFHX1B mutations in patients with Mowat-Wilson syndrome
3. A missense mutation in theZFHX1B gene associated with an atypical Mowat–Wilson syndrome phenotype
4. Intrauterine Constraint and Craniosynostosis
5. Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22-q24.1
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1. Neurological Phenotype of Mowat-Wilson Syndrome;Genes;2021-06-27
2. MOWAT–WILSON SYNDROME;Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30
3. Syndromic Craniosynostosis Can Define New Candidate Genes for Suture Development or Result from the Non-specifc Effects of Pleiotropic Genes: Rasopathies and Chromatinopathies as Examples;Frontiers in Neuroscience;2017-10-18
4. Incontinence and psychological symptoms in individuals with Mowat-Wilson Syndrome;Research in Developmental Disabilities;2017-03
5. Hirschsprung’s disease in children with Mowat–Wilson syndrome;Pediatric Surgery International;2015-07-09
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