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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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Detalles Bibliográficos
Autores principales: CHEN, YONG, YANG, FUWEI, ZHENG, HEXIN, ZHOU, JIANDA, ZHU, GANGHUA, HU, PENG, WU, WEIJING
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768954/
https://www.ncbi.nlm.nih.gov/pubmed/26781036
http://dx.doi.org/10.3892/mmr.2016.4774