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Severe phenotype of X‐linked dominant chondrodysplasia punctata
A prenatally ascertained case representing the more severe end of the X‐linked dominant chondrodysplasia punctata (CDPX2).
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582310/ https://www.ncbi.nlm.nih.gov/pubmed/28878897 http://dx.doi.org/10.1002/ccr3.1008 |
| Sumario: | A prenatally ascertained case representing the more severe end of the X‐linked dominant chondrodysplasia punctata (CDPX2). |
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