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Revista Brasileira de Reumatologia, ISSN 0482-5004, 2017, Volume 57, pp. S308 - S308
Journal Article
Molecular Syndromology, ISSN 1661-8769, 04/2016, Volume 7, Issue 1, pp. 19 - 25
Short stature homeobox gene (SHOX) mutations and pseudoautosomal region 1 (PAR1) deletions encompassing SHOX are known causes of Léri-Weill dyschondrosteosis... 
Original Article | Short stature | SHOX | SHOX duplications | Y chromosome rearrangement | GH-IGF1 axis | Original
Journal Article
Journal of Pediatric and Adolescent Gynecology, ISSN 1083-3188, 04/2018, Volume 31, Issue 2, pp. 138 - 139
Patients’ underlying medical conditions might affect the presentation and progression of an eating disorder. We describe a patient with an undiagnosed, rare,... 
Short stature | Shox gene | Eating disorder | Madelung deformity
Journal Article
Journal of Oral and Maxillofacial Surgery, ISSN 0278-2391, 2018, Volume 77, Issue 4, pp. 762 - 768
One of the most common causes of short stature is a defect of the short stature homeobox-containing (SHOX) gene, which is located in pseudoautosomal region 1... 
GENOTYPES | HOMEOBOX GENE SHOX | DENTISTRY, ORAL SURGERY & MEDICINE | GROWTH | IDIOPATHIC SHORT STATURE | PHENOTYPES | DEFICIENCY | HAPLOINSUFFICIENCY | CHILDREN | Estrogen
Journal Article
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 12/2011, Volume 19, Issue 12, pp. 1218 - 1225
Journal Article
Korean Journal of Pediatrics, ISSN 1738-1061, 10/2017, Volume 60, Issue 10, pp. 327 - 332
PurposeShort stature affects approximately 2%–3% of children, representing one of the most frequent disorders for which clinical attention is sought during... 
SHOX gene | Molecular sequence | Anthropometric measures | Idiopathic short stature
Journal Article
Current Genomics, ISSN 1389-2029, 04/2007, Volume 8, Issue 2, pp. 129 - 136
Journal Article
Cytogenetic and Genome Research, ISSN 1424-8581, 2019, Volume 158, Issue 2, pp. 56 - 62
SHOX resides in the short arm pseudoautosomal region (PAR1) of the sex chromosomes and escapes X inactivation. SHOX haploinsufficiency underlies idiopathic... 
Idiopathic short stature | Leri-Weill dyschondrosteosis | CpG island | ELEMENTS UPSTREAM | IDENTIFICATION | DELETION | REGION | CELL BIOLOGY | Copy number variation | GENE SHOX | DOWNSTREAM | GENETICS & HEREDITY | DNA methylation | REVEALS
Journal Article
by Si, N and Meng, XL and Zhao, Z and Xia, WB and Zhang, X
JOURNAL OF TRANSLATIONAL MEDICINE, ISSN 1479-5876, 04/2019, Volume 17
BackgroundGenomic disorders present a wide spectrum of unrelated clinical entities that result from genomic rearrangements. Interstitial insertions requiring... 
X-linked recessive | MEDICINE, RESEARCH & EXPERIMENTAL | SOX3 | Genu varum | Xq27 | 1 palindrome | SHOX | Interstitial insertion | Pseudoautosomal region 1 | MECHANISMS | REARRANGEMENTS
Journal Article