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A 17q24.3 duplication identified in a large Chinese family with brachydactyly‐anonychia
BACKGROUND: Brachydactyly (BD) is a rare autosomal dominant inherited disease characterized by shortness of the fingers and/or toes, which has been classified into the subtypes A–E. However, the exact cause and mechanism of BD remain to be illuminated. Here, we aim to reveal the clinical and genetic...
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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.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7507485/ https://ncbi.nlm.nih.gov/pubmed/32583964 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1392 |
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