Annals of Pediatric Endocrinology & Metabolism

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Turner syndrome presented with tall stature due to overdosage of the SHOX gene

Go Hun Seo, Eungu Kang, Ja Hyang Cho, Beom Hee Lee, Jin-Ho Choi, Gu-Hwan Kim, Eul-Ju Seo, Han-Wook Yoo

Ann Pediatr Endocrinol Metab. 2015;20(2):110-113. Published online June 30, 2015
DOI: https://doi.org/10.6065/apem.2015.20.2.110

Turner syndrome presented with tall stature due to overdosage of theSHOXgene

Go Hun Seo, Eungu Kang, Ja Hyang Cho, Beom Hee Lee, Jin-Ho Choi, Gu-Hwan Kim, Eul-Ju Seo, Han-Wook Yoo

Annals of Pediatric Endocrinology & Metabolism. 2015;20(2):110

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The Phenotype of Short Stature Homeobox Gene (SHOX) Deficiency in Childhood: Contrasting Children With Leri-Weill Dyschondrosteosis and Turner Syndrome

J.A. Stockman

Yearbook of Pediatrics. 2007;2007:125-127

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Growth Hormone Therapy in Children with Turner Syndrome, Noonan Syndrome, and SHOX Gene Mutations

Philippe F. Backeljauw, Iris Gutmark-Little

Pediatric Endocrinology. 2018;113-144

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Rare inheritance of Leri-Weill Syndrome due to crossover of short stature Homeobox Gene (SHOX) Deletions between X and Y Chromosomes: a case report

Marisa Censani, Kwame Anyane-Yeboa, Ronald Wapner, Erica Spiegel, Edwin Guzman, Sharon E Oberfield

International Journal of Pediatric Endocrinology. 2013;2013(1):

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Trisomy of the short stature homeobox-containing gene (SHOX ), resulting from a duplication-deletion of the X chromosome

K. A. Adamson, I. Cross, J. A. Batch, G. A. Rappold, I. A. Glass, S. G. Ball

Clinical Endocrinology. 2002;56(5):671-675

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SHOXgene is expressed in vertebral body growth plates in idiopathic and congenital scoliosis: Implications for the etiology of scoliosis in turner syndrome

Gregory Day, Attila Szvetko, Lyn Griffiths, I. Bruce McPhee, John Tuffley, Robert LaBrom, Geoffrey Askin, Peter Woodland, Eamonn McClosky, Ian Torode, Francis Tomlinson

Journal of Orthopaedic Research. 2008;27(6):807-813

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SHOX gene in Leri-Weill syndrome and in idiopathic short stature

Sergio Bernasconi, S. Mariani, C. Falcinelli, S. Milioli, L. Iughetti, A. Forabosco

Journal of Endocrinological Investigation. 2001;24(9):737-741

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The Phenotype of Short Stature Homeobox Gene (SHOX) Deficiency in Childhood: Contrasting Children with Leri-Weill Dyschondrosteosis and Turner Syndrome

Judith L. Ross, Karen Kowal, Charmian A. Quigley, Werner F. Blum, Gordon B. Cutler, Brenda Crowe, Karine Hovanes, Frederick F. Elder, Andrew R. Zinn

The Journal of Pediatrics. 2005;147(4):499-507

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The role of the SHOX gene in the pathophysiology of Turner syndrome

Conceicao S. Oliveira, Cresio Alves

Endocrinología y Nutrición. 2011;58(8):433-442

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Detection of SHOX gene deletions in Egyptian children with idiopathic short stature using FISH

Amr Shujaa-Addin, Mervat Hashish, Nahla Nazmy, Amany Srour, Ebtesam Abdalla

Meta Gene. 2020;24:100697

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