Identity Defect in melanocyte development; one of the first genetic disorders for which a pedigree was presented in 1786. Inheritance Autosomal dominant; frequency is about 2.5/105 newborns.
Piebaldism / L. Larizza, A. Beghini. - In: ATLAS OF GENETICS AND CYTOGENETICS IN ONCOLOGY AND HAEMATOLOGY. - ISSN 1768-3262. - 4:3(2000 Jun), pp. 157-158. [10.4267/2042/37657]
Piebaldism
L. LarizzaPrimo
;A. BeghiniUltimo
2000
Abstract
Identity Defect in melanocyte development; one of the first genetic disorders for which a pedigree was presented in 1786. Inheritance Autosomal dominant; frequency is about 2.5/105 newborns.
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