A carregar...
FGFR3 mutation frequency in 324 cases from the International Skeletal Dysplasia Registry
Fibroblast growth factor receptor 3 (FGFR3) is the only gene known to cause achondroplasia (ACH), hypochondroplasia (HCH), and thanatophoric dysplasia types I and II (TD I and TD II). A second, as yet unidentified, gene also causes HCH. In this study, we used sequencing analysis to determine the fre...
Na minha lista:
| Publicado no: | Mol Genet Genomic Med |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BlackWell Publishing Ltd
2014
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4303219/ https://ncbi.nlm.nih.gov/pubmed/25614871 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.96 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|