Detalhe da pesquisa
1.
Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with "Corner Fractures".
Am J Hum Genet
; 101(5): 815-823, 2017 Nov 02.
Artigo
Inglês
| MEDLINE | ID: mdl-29100092
2.
Phenotypic variability of osteogenesis imperfecta type V caused by an IFITM5 mutation.
J Bone Miner Res
; 28(7): 1523-30, 2013 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-23408678
3.
Disease gene characterization through large-scale co-expression analysis.
PLoS One
; 4(12): e8491, 2009 Dec 31.
Artigo
Inglês
| MEDLINE | ID: mdl-20046828
4.
Genetic determinants of osteoporosis susceptibility in a female Ashkenazi Jewish population.
Genet Med
; 6(1): 33-7, 2004.
Artigo
Inglês
| MEDLINE | ID: mdl-14726807