A Comprehensive Genetic and Clinical Evaluation of Waardenburg Syndrome Type II in a Set of Iranian Patients

Waardenburg syndrome (WS) is a neurocristopathy with an autosomal dominant mode of inheritance, and considerable clinical and genetic heterogeneity. WS type II is the most common type of WS in many populations presenting with sensorineural hearing impairment, heterochromia iridis, hypoplastic blue e...

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Detalles Bibliográficos
Autores principales: Jalilian, Nazanin, Tabatabaiefar, Mohammad Amin, Yazdanpanah, Mahboubeh, Darabi, Elham, Bahrami, Tayyeb, Zekri, Ali, Noori-Daloii, Mohammad Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Babol University of Medical Sciences 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134422/
https://www.ncbi.nlm.nih.gov/pubmed/30234069
http://dx.doi.org/10.22088/IJMCM.BUMS.7.1.17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134422/
https://www.ncbi.nlm.nih.gov/pubmed/30234069
http://dx.doi.org/10.22088/IJMCM.BUMS.7.1.17

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