Trisomy of the Short Stature Homeobox-Containing Gene (SHOX) due to Duplication/Deletion of the X Chomosome: Clinical Implications on the Stature-Reference-Cited by-同舟云学术

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Trisomy of the Short Stature Homeobox-Containing Gene (SHOX) due to Duplication/Deletion of the X Chomosome: Clinical Implications on the Stature

Published:2010 Issue:4 Volume:74 Page:297-304
ISSN:1663-2826
Container-title:Hormone Research in Paediatrics
language:en
Short-container-title:Horm Res Paediatr

Author:

del Rey Graciela,Jasper Héctor,Bengolea Sonia Viviana,Boywitt Adriana,De Bellis Rodolfo,Heinrich Juan Jorge

Publisher

S. Karger AG

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A 105 kb interstitial insertion in the Xq27.1 palindrome from pseudoautosomal region PAR1 causes a novel X-linked recessive compound phenotype;Journal of Translational Medicine;2019-04-29

2. SHOX Duplication and Tall Stature in a Patient with Xq Deletion and Vascular Disease;Case Reports in Genetics;2019-04-08

3. Comparison of SHOX and associated elements duplications distribution between patients (Lėri-Weill dyschondrosteosis/idiopathic short stature) and population sample;Gene;2017-09

4. Short stature homeobox-containing gene duplications in 3.7% of girls with tall stature and normal karyotypes;Acta Paediatrica;2017-07-20

5. Turner syndrome caused by rare complex structural abnormalities involving chromosome X;Experimental and Therapeutic Medicine;2017-07-10

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