Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations.
about
Genetic analysis of osteogenesis imperfecta in the Palestinian population: molecular screening of 49 affected families.Mutations That Alter the Carboxy-Terminal-Propeptide Cleavage Site of the Chains of Type I Procollagen Are Associated With a Unique Osteogenesis Imperfecta Phenotype.Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies
P2860
Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations.
description
2016 nî lūn-bûn
@nan
2016 թվականի օգոստոսի 30-ին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
name
Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations.
@en
Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations.
@nl
type
label
Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations.
@en
Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations.
@nl
prefLabel
Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations.
@en
Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations.
@nl
P2093
P2860
P356
P1476
Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations.
@en
P2093
Ann Dalton
Emma A Webb
Emma Hobson
Farhan Ali
Glenda J Sobey
M Zulf Mughal
Nicholas J Bishop
Nick J Shaw
Paul Arundel
Rebecca C Pollitt
P2860
P304
P356
10.1002/AJMG.A.37958
P407
P577
2016-08-30T00:00:00Z