SciELO - Brasil - Baixa estatura por haploinsuficiência do gene SHOX: do diagnóstico ao tratamento Baixa estatura por haploinsuficiência do gene SHOX: do diagnóstico ao tratamento
Hormones.gr
A Track Record on SHOX: From Basic Research to Complex Models and Therapy
SHOX Haploinsufficiency as a Cause of Syndromic and Nonsyndromic Short Stature | Semantic Scholar
SHOX Gene - GeneCards | SHOX Protein | SHOX Antibody
Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency | EMBO Molecular Medicine
CytoCell SHOX FISH Probe | OGT
Clinical impact of variants in non-coding regions of SHOX – Current knowledge - ScienceDirect
a) Illustration of the SHOX gene deletion. The schematic illustrates... | Download Scientific Diagram
SHOX in Short Stature Syndromes | Semantic Scholar
SHOX Deficiency - Child Growth Foundation
The SHOX gene. The SHOX gene maps to 505–527 kb from the telomere of... | Download Scientific Diagram
SHOX haploinsufficiency presenting with isolated short long bones in the second and third trimester | European Journal of Human Genetics
RUO - SHOX / SE X - ISH Probes - Molecular Pathology
Learn more about TS and... - Turner Syndrome Global Alliance | Facebook
Identification of a limb enhancer that is removed by pathogenic deletions downstream of the SHOX gene | Scientific Reports
Universitätsklinikum Heidelberg: SHOX-Database
Frontiers | Identification and Tissue-Specific Characterization of Novel SHOX-Regulated Genes in Zebrafish Highlights SOX Family Members Among Other Genes
The role of the SHOX gene in the pathophysiology of Turner syndrome. | Semantic Scholar
Mechanisms regulating SHOX gene expression. A, Alternative promoters.... | Download Scientific Diagram
SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators | Italian Journal of Pediatrics | Full Text
Full article: SHOX at a glance: from gene to protein
Journal of Case studies | Juniper Publishers
