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Report of two Japanese patients with piebaldism including a novel mutation in KIT
Download from onlinelibrary.wiley.comFive novel mutations in SASH1 contribute to lentiginous phenotypes in Japanese families
Download from onlinelibrary.wiley.comIncontinentia pigmenti with retinal vascular anomaly and deletion of exons 4-10 in NEMO
Download from api.wiley.comGenetic analyses of oculocutaneous albinism types 2 and 4 with eight novel mutations
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