Associated Papers
[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
Review and update of mutations causing Waardenburg syndrome.
Pingault V et al.
Human Mutation, 2010
A French CDK4-positive melanoma family with a co-inherited EDNRB mutation.
Soufir N et al.
Journal of Dermatological Science, 2007
Association between endothelin receptor B nonsynonymous variants and melanoma risk.
Soufir N et al.
Journal of the National Cancer Institute, 2005
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