Mutations that Cause Osteoglophonic Dysplasia Define Novel Roles for FGFR1 in Bone Elongation

Activating mutations in the genes for fibroblast growth factor receptors 1–3 (FGFR1–3) are responsible for a diverse group of skeletal disorders. In general, mutations in FGFR1 and FGFR2 cause the majority of syndromes involving craniosynostosis, whereas the dwarfing syndromes are largely associated...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: White, Kenneth E., Cabral, Jose M., Davis, Siobhan I., Fishburn, Tonya, Evans, Wayne E., Ichikawa, Shoji, Fields, Joanna, Yu, Xijie, Shaw, Nick J., McLellan, Neil J., McKeown, Carole, FitzPatrick, David, Yu, Kai, Ornitz, David M., Econs, Michael J.
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society of Human Genetics 2005
Assuntos:
Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1196382/
https://ncbi.nlm.nih.gov/pubmed/15625620
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados