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Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report
Split hand/foot malformation (SHFM) or ectrodactyly is a rare genetic condition affecting limb development. SHFM shows clinical and genetic heterogeneity. It can present as an isolated form or in combination with additional anomalies affecting the long bones (nonsyndromic form) or other organ system...
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| Gepubliceerd in: | Mol Syndromol |
|---|---|
| Hoofdauteurs: | , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
S. Karger AG
2016
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4802982/ https://ncbi.nlm.nih.gov/pubmed/27022330 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000443708 |
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