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Mid1/Mid2 expression in craniofacial development and a literature review of X‐linked opitz syndrome
BACKGROUND: Opitz syndrome (OS) is a genetic disorder that affects mainly the development of midline structures, including the craniofacial region, embryonic heart, and urogenital system. The manifestations of X‐linked OS are believed to be results of a malfunctioned gene, MID1, whose product has be...
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| Publicado no: | Mol Genet Genomic Med |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4707030/ https://ncbi.nlm.nih.gov/pubmed/26788540 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.183 |
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