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Fibrochondrogenesis 2
- ... disorder in the family. FBCG1 FBCG2 Fibrochondrogenesis-1 Fibrochondrogenesis-2 Genetic Testing Registry: Fibrochondrogenesis 1 Genetic Testing Registry: ...
- ... COL11A2 gene have been identified in people with fibrochondrogenesis type 2, a disorder of bone growth characterized by severe skeletal abnormalities and hearing loss. Infants with fibrochondrogenesis type 2 have a very narrow chest that prevents the ...
- ... letter to the editor regarding the mechanism underlying fibrochondrogenesis. Gene. 2013 Oct 10;528(2):367-8. doi: 10.1016/j.gene.2013. ... F, Alshammari MJ, Alkuraya FS. Molecular pathogenesis of fibrochondrogenesis: is ... deficiency? Gene. 2012 Dec 15;511(2):480-1. doi: 10.1016/j.gene.2012. ...