about
The Human Pseudoautosomal Region (PAR): Origin, Function and FutureIdentification of a major recombination hotspot in patients with short stature and SHOX deficiency.High incidence of SHOX anomalies in individuals with short stature.SHOX at a glance: from gene to protein.A Track Record on SHOX: From Basic Research to Complex Models and TherapyPseudodominant inheritance of Langer mesomelic dysplasia caused by a SHOX homeobox missense mutation.Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri-Weill dyschondrosteosis.Genotype-Phenotype Relationship in Patients and Relatives with SHOX Region Anomalies in the French Population.SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome.Identification of a novel SHOX mutation in a Chinese family with isolated Madelung deformity.Short stature homeoboxcontaining gene and idiopathic short stature
P2860
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P2860
description
2001 nî lūn-bûn
@nan
2001 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
SHOX point mutations in dyschondrosteosis
@ast
SHOX point mutations in dyschondrosteosis
@en
SHOX point mutations in dyschondrosteosis
@nl
type
label
SHOX point mutations in dyschondrosteosis
@ast
SHOX point mutations in dyschondrosteosis
@en
SHOX point mutations in dyschondrosteosis
@nl
prefLabel
SHOX point mutations in dyschondrosteosis
@ast
SHOX point mutations in dyschondrosteosis
@en
SHOX point mutations in dyschondrosteosis
@nl
P2093
P3181
P356
P1476
SHOX point mutations in dyschondrosteosis
@en
P2093
P3181
P356
10.1136/JMG.38.5.323
P407
P577
2001-05-01T00:00:00Z