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Mowat-Wilson syndrome in a Moroccan consanguineous family

Mowat-Wilson syndrome is a mental retardation-multiple congenital anomaly syndrome characterized by a typical facies, developmental delay, epilepsy, and variable congenital malformations, including Hirschsprung disease, urogenital anomalies, congenital heart disease, and agenesis of the corpus callo...

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Bibliografski detalji
Glavni autori: Ratbi, Ilham, Elalaoui, Chafai Siham, Dastot-Le, Moal Florence, Goossens, Michel, Giurgea, Irina, Sefiani, Abdelaziz
Format: Artigo
Jezik:Inglês
Izdano: Medknow Publications 2007
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3168139/
https://ncbi.nlm.nih.gov/pubmed/21957361
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.38988
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