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Clinical and genetic investigation of families with type II Waardenburg syndrome
The present study aimed to investigate the molecular pathology of Waardenburg syndrome type II in three families, in order to provide genetic diagnosis and hereditary counseling for family members. Relevant clinical examinations were conducted on the probands of the three pedigrees. Peripheral blood...
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| Publicado no: | Mol Med Rep |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4768954/ https://ncbi.nlm.nih.gov/pubmed/26781036 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2016.4774 |
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