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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Detalles Bibliográficos
Autores principales: Wang, Li, Qin, Litao, Li, Tao, Liu, Hongjian, Ma, Lingcao, Li, Wan, Wu, Dong, Wang, Hongdan, Guo, Qiannan, Guo, Liangjie, Liao, Shixiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780116/
https://www.ncbi.nlm.nih.gov/pubmed/29115496
http://dx.doi.org/10.3892/mmr.2017.7874

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780116/
https://www.ncbi.nlm.nih.gov/pubmed/29115496
http://dx.doi.org/10.3892/mmr.2017.7874

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