Acanthosis nigricans and hypochondroplasia in a child with a K650Q mutation in FGFR3.

Autor: Berk DR; Departments of Internal Medicine and Pediatrics, Division of Dermatology, Washington University School of Medicine and St. Louis Children’s Hospital, St. Louis, Missouri 63110, USA. dberk@dom.wustl.edu, Boente Mdel C, Montanari D, Toloza MG, Primc NB, Prado MI, Bayliss SJ, Pique LM, Schrijver I

Publikováno v: Pediatric dermatology [Pediatr Dermatol] 2010 Nov-Dec; Vol. 27 (6), pp. 664-6.