Learn more about TS and... - Turner Syndrome Global Alliance | Facebook
Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency | EMBO Molecular Medicine
37.2 Structure of the SHOX gene and cDNA. This figure shows the... | Download Scientific Diagram
Detection of SHOX gene deletions in Egyptian children with idiopathic short stature using FISH - ScienceDirect
The role of the SHOX gene in the pathophysiology of Turner syndrome. | Semantic Scholar
Frontiers | Heterozygous Deletion of the SHOX Gene Enhancer in two Females With Clinical Heterogeneity Associating With Skewed XCI and Escaping XCI
SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators | Italian Journal of Pediatrics | Full Text
SHOX haploinsufficiency presenting with isolated short long bones in the second and third trimester | European Journal of Human Genetics
Frontiers | Identification and Tissue-Specific Characterization of Novel SHOX-Regulated Genes in Zebrafish Highlights SOX Family Members Among Other Genes
Mechanisms regulating SHOX gene expression. A, Alternative promoters.... | Download Scientific Diagram
SHOX Gene - GeneCards | SHOX Protein | SHOX Antibody
a) Illustration of the SHOX gene deletion. The schematic illustrates... | Download Scientific Diagram
SHOX Haploinsufficiency as a Cause of Syndromic and Nonsyndromic Short Stature | Semantic Scholar
Chromosomal localization, genomic structures and cDNA forms of the SHOX... | Download Scientific Diagram
RUO - SHOX / SE X - ISH Probes - Molecular Pathology
Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency | EMBO Molecular Medicine
Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location | Journal of Medical Genetics
Journal of Case studies | Juniper Publishers
Hormones.gr
SciELO - Brasil - Genetic causes of isolated short stature Genetic causes of isolated short stature
The SHOX gene. The SHOX gene maps to 505–527 kb from the telomere of... | Download Scientific Diagram
The role of the SHOX gene in the pathophysiology of Turner syndrome | Endocrinología y Nutrición
Identification of a novel SHOX mutation in a Chinese family with isolated Madelung deformity | SpringerLink
