CrossRef Text and Data Mining
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Screening of SHOX gene sequence variants in Saudi Arabian children with idiopathic short stature
Abdulla A. Alharthi, Ehab I. El-Hallous, Iman M. Talaat, Hamed A. Alghamdi, Matar I. Almalki, Ahmed Gaber
Clin Exp Pediatr. 2017;60(10):327-332.   Published online October 20, 2017
DOI: https://doi.org/10.3345/kjp.2017.60.10.327

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Screening of SHOX gene sequence variants in Saudi Arabian children with idiopathic short stature
Korean Journal of Pediatrics. 2017;60(10):327   Crossref logo
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Detection of SHOX gene deletions in Egyptian children with idiopathic short stature using FISH
Meta Gene. 2020;24:100697   Crossref logo
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SHOX variations in Idiopathic Short Stature in North India and its overall prevalence in Asia
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Short stature and SHOX (Short stature homeobox) variants—efficacy of screening using various strategies
PeerJ. 2020;8:e10236   Crossref logo
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Comparison of SHOX and associated elements duplications distribution between patients (Lėri-Weill dyschondrosteosis/idiopathic short stature) and population sample
Gene. 2017;627:164-168   Crossref logo
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SHOX gene in Leri-Weill syndrome and in idiopathic short stature
Journal of Endocrinological Investigation. 2001;24(9):737-741   Crossref logo
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Detection of Del/Dup Inside SHOX/PAR1 Region in Children and Young Adults with Idiopathic Short Stature
Genes. 2021;12(10):1546   Crossref logo
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Heterozygous Deletion in Exons 4-5 of SHOX Gene in a Patient Diagnosed as Idiopathic Short Stature
Acta Medica Marisiensis. 2017;63(3):155-158   Crossref logo
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The Phenotype of Short Stature Homeobox Gene (SHOX) Deficiency in Childhood: Contrasting Children With Leri-Weill Dyschondrosteosis and Turner Syndrome
Yearbook of Pediatrics. 2007;2007:125-127   Crossref logo
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SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Léri–Weill dyschondrosteosis
Gene. 2012;491(2):123-127   Crossref logo
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