Results 151 to 160 of about 880 (178)
Some of the next articles are maybe not open access.

Piebaldism in children.

Cutis, 2017
Piebaldism is a rare autosomal-dominant disorder of melanocyte development characterized by congenital poliosis and stable patches of leukoderma. Initially, these clinical features may be the presenting signs of various syndromes or associated diseases, which should be considered in the differential diagnosis.
Alexandra, Grob, Steven, Grekin
openaire   +1 more source

A PIEBALD FAMILY

Biometrika, 1938
openaire   +1 more source

New KIT mutations in patients with piebaldism

Journal of Dermatological Science, 2004
Naoki Oiso, Amy S Paller
exaly  

Piebaldism

2019
Jovan Lalošević, Miloš Nikolić
openaire   +1 more source

Piebaldism: an autonomous autosomal dominant entity

Clinical Genetics, 1991
Íngrid Winship   +2 more
exaly  

Piebaldism

2009
Markus Braun-Falco   +199 more
openaire   +1 more source

(16) Piebaldism

British Journal of Dermatology, 2006
D.R. Taylor, T. Robinson
openaire   +1 more source

Piebaldism with deafness: Molecular evidence for an expanded syndrome

American Journal of Medical Genetics Part A, 1998
Richard A Spritz, P Beighton
exaly  

Piebaldism.

The British journal of dermatology, 1976
D R, Taylor, T, Robinson
openaire   +1 more source

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