Associated Papers
Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China.
Wu H et al.
Plos One, 2016
[Hereditary hypomelanocytoses: the role of PAX3, SOX10, MITF, SNAI2, KIT, EDN3 and EDNRB genes].
Otręba M et al.
Postepy Higieny I Medycyny Doswiadczalnej (online), 2013
Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophy.
Kapoor S et al.
Molecular Vision, 2012
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