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

David R Berk1, Maria Del Carmen Boente, Daniela Montanari

  • 1Departments 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

Pediatric Dermatology
|April 22, 2011
PubMed

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