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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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| 主要な著者: | , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Medknow Publications
2007
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| 主題: | |
| オンライン･アクセス: | 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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