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Mowat-Wilson Syndrome: The First Clinical and Molecular Report of an Indonesian Patient
Mowat-Wilson syndrome (OMIM 235730) is a genetic condition characterized by moderate-to-severe intellectual disability, a recognizable facial phenotype, and multiple congenital anomalies. The striking facial phenotype in addition to other features such as severely impaired speech, hypotonia, microce...
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| Главные авторы: | , , , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Hindawi Publishing Corporation
2012
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3517822/ https://ncbi.nlm.nih.gov/pubmed/23243526 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/949507 |
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