Genetic disorders of pigmentation
Author:
Publisher
Elsevier BV
Subject
Dermatology
Reference97 articles.
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4. Deletion of the c-kit protooncogene in the human developmental defect piebald trait;Fleischman;Proc. Natl. Acad. Sci. U. S. A.,1991
5. Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism;Giebel;Proc. Natl. Acad. Sci. U. S. A.,1991
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