Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia.
about
Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome)Clinical features of hereditary progressive arthro-ophthalmopathy (Stickler syndrome): a survey.The ocular manifestations of Weissenbacher-Zweymuller syndrome.
P2860
Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia.
description
1992 nî lūn-bûn
@nan
1992 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia.
@ast
Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia.
@en
type
label
Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia.
@ast
Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia.
@en
prefLabel
Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia.
@ast
Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia.
@en
P2093
P356
P1476
Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia.
@en
P2093
P304
P356
10.1002/AJMG.1320430616
P577
1992-08-01T00:00:00Z