SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasia.
about
Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasiaAmino acid substitutions of conserved residues in the carboxyl-terminal domain of the alpha 1(X) chain of type X collagen occur in two unrelated families with metaphyseal chondrodysplasia type SchmidGenetic aspects of familial osteoarthritisIdentification of a locus for a form of spondyloepiphyseal dysplasia on chromosome 15q26.1: exclusion of aggrecan as a candidate geneFrom collagen chemistry towards cell therapy - a personal journey.
P2860
SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasia.
description
1992 nî lūn-bûn
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1992 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հոտեմբերին 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
SSCP and segregation analysis ...... ble forms of chondrodysplasia.
@ast
SSCP and segregation analysis ...... ble forms of chondrodysplasia.
@en
type
label
SSCP and segregation analysis ...... ble forms of chondrodysplasia.
@ast
SSCP and segregation analysis ...... ble forms of chondrodysplasia.
@en
prefLabel
SSCP and segregation analysis ...... ble forms of chondrodysplasia.
@ast
SSCP and segregation analysis ...... ble forms of chondrodysplasia.
@en
P2093
P2860
P1476
SSCP and segregation analysis ...... ble forms of chondrodysplasia.
@en
P2093
Beighton P
Boot-Handford R
Sweetman WA
P2860
P304
P407
P577
1992-10-01T00:00:00Z