Waardenburg syndrome (WS)

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URI: http://hdl.handle.net/2042/38200  |   DOI : https://doi.org/10.4267/2042/38200
Title: Waardenburg syndrome (WS)
Author: Vicente-Dueñas, C; Bermejo-Rodrîguez, C; Pérez-Caro, M; González-Herrero, I; Sánchez-Martîn, M; Sánchez-Garcîa, I
Description: Review on Waardenburg syndrome (WS), with data on clinics, and the genes involved.
Subject: Chromosome 2; Chromosome 3; Chromosome 8; Chromosome 13; Chromosome 20; Chromosome 22; Klein-Waardenburg syndrome (WS3) (alias); Waardenburg syndrome with upper limb anomalies (WS3) (alias); White forelock with malformations (WS3) (alias); Waardenburg-Hirschsprung disease (WS4) (alias); Waardenburg syndrome variant (WS4) (alias); Shan-Waardenburg syndrome (WS4) (alias); Hirschsprung disease with pigmentary anomaly (WS4) (alias); Cancer Prone Diseases Section; Endothelin-3; MITF protein, human; PAX3 protein, human; Receptor, Endothelin B; SOX10 protein, human; snail family transcription factors; Abnormalities, Multiple; Myosarcoma; Neoplasms, Connective and Soft Tissue; Neoplasms, Muscle Tissue; Rhabdomyosarcoma; Sarcoma; Waardenburg's Syndrome
Publisher: Jean-Loup Huret (Editor-in-Chief) ; INIST-CNRS (Publisher)
Date: 2005

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