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Familiar del3p syndrome: The uncertainty of the prognosis. A case report
The 3p deletion syndrome is an unusual condition. The few cases described are mainly de novo. We described a familial case detected in a prenatal diagnosis. Three members of the family had the 3p26.3‐p26.1 deletion; however, only the son presented clinical features.
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077371/ https://www.ncbi.nlm.nih.gov/pubmed/33936696 http://dx.doi.org/10.1002/ccr3.4036 |