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Hearing Loss in Syndromic Craniosynostoses: Introduction and Consideration of Mechanisms

PURPOSE: There are a number of craniosynostosis syndromes with hearing loss—including Muenke, Apert, Pfeiffer, Crouzon, Beare-Stevenson, Crouzon with acanthosis nigricans, and Jackson-Weiss syndromes—that result from mutations in the fibroblast growth factor receptor (FGFR) genes. Studies of FGFRs a...

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Main Authors: Agochukwu, Nneamaka B., Solomon, Benjamin D., Muenke, Maximilian
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4131981/
https://ncbi.nlm.nih.gov/pubmed/24686979
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1044/2014_AJA-13-0036
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