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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707030/ https://www.ncbi.nlm.nih.gov/pubmed/26788540 http://dx.doi.org/10.1002/mgg3.183 |