Detalhe da pesquisa
1.
Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis.
Nat Genet
; 36(4): 405-10, 2004 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-14991055
2.
Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome.
Am J Hum Genet
; 84(4): 542-9, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19361615
3.
Analysis of clones from a human cartilage cDNA library provides insight into chondrocyte gene expression and identifies novel candidate genes for the osteochondrodysplasias.
Mol Genet Metab
; 79(1): 34-42, 2003 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-12765844