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Mutation analysis of Crouzon syndrome in Taiwanese patients

Crouzon syndrome is an autosomal‐dominant disorder that causes premature fusion of the cranial suture. Crouzon, Pfeiffer, and Apert syndromes are caused by mutations in the extracellular, third immunoglobulin‐like domain, and adjacent linker regions (exons IIIa and IIIc) of the fibroblast growth fac...

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Détails bibliographiques
Publié dans:J Clin Lab Anal
Auteurs principaux: Chang, Chin‐Ping, Wan, Lei, Tsai, Chang‐Hai, Lee, Cheng‐Chun, Tsai, Fuu‐Jen
Format: Artigo
Langue:Inglês
Publié: Wiley Subscription Services, Inc., A Wiley Company 2006
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6807587/
https://ncbi.nlm.nih.gov/pubmed/16470531
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.20096
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