Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22
about
Mutations in the human TBX4 gene cause small patella syndrome.Identical mutations in NOG can cause either tarsal/carpal coalition syndrome or proximal symphalangismMeier-Gorlin syndrome: report of eight additional cases and review.Genetic basis of hindlimb loss in a naturally occurring vertebrate model.Genitopatellar syndrome: a recognizable phenotype.International nosology and classification of constitutional disorders of bone (2001).
P2860
Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22
description
1999 nî lūn-bûn
@nan
1999 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Localization of a gene for fam ...... (PTLAH) to chromosome 17q21-22
@ast
Localization of a gene for fam ...... (PTLAH) to chromosome 17q21-22
@en
Localization of a gene for familial patella aplasia-hypoplasia
@nl
type
label
Localization of a gene for fam ...... (PTLAH) to chromosome 17q21-22
@ast
Localization of a gene for fam ...... (PTLAH) to chromosome 17q21-22
@en
Localization of a gene for familial patella aplasia-hypoplasia
@nl
prefLabel
Localization of a gene for fam ...... (PTLAH) to chromosome 17q21-22
@ast
Localization of a gene for fam ...... (PTLAH) to chromosome 17q21-22
@en
Localization of a gene for familial patella aplasia-hypoplasia
@nl
P2093
P2860
P356
P1476
Localization of a gene for fam ...... (PTLAH) to chromosome 17q21-22
@en
P2093
P2860
P304
P356
10.1086/302505
P407
P577
1999-08-01T00:00:00Z