Detection of SHOX gene deletions in Egyptian children with idiopathic short stature using FISH - ScienceDirect
Hormones.gr
Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency | EMBO Molecular Medicine
Mechanisms regulating SHOX gene expression. A, Alternative promoters.... | Download Scientific Diagram
a) Illustration of the SHOX gene deletion. The schematic illustrates... | Download Scientific Diagram
Frontiers | Identification and Tissue-Specific Characterization of Novel SHOX-Regulated Genes in Zebrafish Highlights SOX Family Members Among Other Genes
Learn more about TS and... - Turner Syndrome Global Alliance | Facebook
Universitätsklinikum Heidelberg: SHOX-Database
SciELO - Brasil - Baixa estatura por haploinsuficiência do gene SHOX: do diagnóstico ao tratamento Baixa estatura por haploinsuficiência do gene SHOX: do diagnóstico ao tratamento
SHOX Gene - GeneCards | SHOX Protein | SHOX Antibody
The role of the SHOX gene in the pathophysiology of Turner syndrome. | Semantic Scholar
CytoCell SHOX FISH Probe | OGT
Identification of a novel SHOX mutation in a Chinese family with isolated Madelung deformity | SpringerLink
SHOX haploinsufficiency presenting with isolated short long bones in the second and third trimester | European Journal of Human Genetics
37.2 Structure of the SHOX gene and cDNA. This figure shows the... | Download Scientific Diagram
italic>SHOX</italic> at a glance: from gene to protein
The role of the SHOX gene in the pathophysiology of Turner syndrome. | Semantic Scholar
SHOX Haploinsufficiency as a Cause of Syndromic and Nonsyndromic Short Stature | Semantic Scholar
Frontiers | Heterozygous Deletion of the SHOX Gene Enhancer in two Females With Clinical Heterogeneity Associating With Skewed XCI and Escaping XCI
RUO - SHOX / SE X - ISH Probes - Molecular Pathology
Identification of a limb enhancer that is removed by pathogenic deletions downstream of the SHOX gene | Scientific Reports
Journal of Case studies | Juniper Publishers
The role of the SHOX gene in the pathophysiology of Turner syndrome | Endocrinología y Nutrición
Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency | EMBO Molecular Medicine
SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators | Italian Journal of Pediatrics | Full Text
