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Two brothers with the Marden-Walker syndrome: case report and review
Two brothers with blepharophimosis, congenital joint contractures, and mental retardation characteristic of the Marden-Walker syndrome are described. This sib pair strengthens the case for autosomal recessive inheritance of the syndrome.
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| Autores principales: | , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
1981
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1048658/ https://ncbi.nlm.nih.gov/pubmed/7252998 |
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