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Mutations in the Homeodomain of HOXD13 Cause Syndactyly Type 1-c in Two Chinese Families
BACKGROUND: Syndactyly type 1 (SD1) is an autosomal dominant limb malformation characterized in its classical form by complete or partial webbing between the third and fourth fingers and/or the second and third toes. Its four subtypes (a, b, c, and d) are defined based on variable phenotypes, but th...
| Autores principales: | , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2014
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4006867/ https://www.ncbi.nlm.nih.gov/pubmed/24789103 http://dx.doi.org/10.1371/journal.pone.0096192 |