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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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| Vydáno v: | J Clin Lab Anal |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Wiley Subscription Services, Inc., A Wiley Company
2006
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| Témata: | |
| On-line přístup: | 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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