Caricamento...
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...
Salvato in:
| Pubblicato in: | J Clin Lab Anal |
|---|---|
| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Wiley Subscription Services, Inc., A Wiley Company
2006
|
| Soggetti: | |
| Accesso online: | 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 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|