Associated Papers
Decoding the mechanisms of cooperative DNA binding by the Paired-like homeodomain family.
Cain B et al.
Biorxiv : the Preprint Server for Biology, 2025
41279221 (PubMed )
Supplement: media-2.xlsx › SuppTable2
Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetrance.
Tooze RS et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2023
37154149 (PubMed )
Supplement: mmc2.pdf
Screening of SHOX gene sequence variants in Saudi Arabian children with idiopathic short stature.
Alharthi AA et al.
Korean Journal of Pediatrics, 2017
Detection of SHOX gene aberrations in routine diagnostic practice and evaluation of phenotype scoring form effectiveness.
Hirschfeldova K et al.
Journal of Human Genetics, 2017
A Track Record on SHOX: From Basic Research to Complex Models and Therapy.
Marchini A et al.
Endocrine Reviews, 2016
The novel human SHOX allelic variant database.
Niesler B et al.
Human Mutation, 2007
Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiency.
Rappold G et al.
Journal of Medical Genetics, 2007
Growth hormone is effective in treatment of short stature associated with short stature homeobox-containing gene deficiency: Two-year results of a randomized, controlled, multicenter trial.
Blum WF et al.
The Journal of Clinical Endocrinology and Metabolism, 2007
Alteration of DNA binding, dimerization, and nuclear translocation of SHOX homeodomain mutations identified in idiopathic short stature and Leri-Weill dyschondrosteosis.
Schneider KU et al.
Human Mutation, 2005
SHOX haploinsufficiency and Leri-Weill dyschondrosteosis: prevalence and growth failure in relation to mutation, sex, and degree of wrist deformity.
Binder G et al.
The Journal of Clinical Endocrinology and Metabolism, 2004
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