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Prenatal diagnosis and genetic counseling for Waardenburg syndrome type I and II in Chinese families
Waardenburg syndrome (WS) is an auditory-pigmentary disorder with varying combinations of sensorineural hearing loss and abnormal pigmentation. The present study aimed to investigate the underlying molecular pathology and provide a method of prenatal diagnosis of WS in Chinese families. A total of 1...
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| Publicado no: | Mol Med Rep |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5780116/ https://ncbi.nlm.nih.gov/pubmed/29115496 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2017.7874 |
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