|
|
| CrossRef Text and Data Mining | |
| Result of CrossRef Text and Data Mining Search is the related articles with entitled article. If you click link1 or link2 you will be able to reach the full text site of selected articles; however, some links do not show the full text immediately at now. If you click CrossRef Text and Data Mining Download icon, you will be able to get whole list of articles from literature included in CrossRef Text and Data Mining. | |
| Turner syndrome presented with tall stature due to overdosage of the |
|
| 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 Annals of Pediatric Endocrinology & Metabolism. 2015;20(2):110  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 Growth Hormone Therapy in Children with Turner Syndrome, Noonan Syndrome, and SHOX Gene Mutations Pediatric Endocrinology. 2018;113-144 Trisomy of the short stature homeobox-containing gene (SHOX
), resulting from a duplication-deletion of the X chromosome Clinical Endocrinology. 2002;56(5):671-675 Rare inheritance of Leri-Weill Syndrome due to crossover of short stature Homeobox Gene (SHOX) Deletions between X and Y Chromosomes: a case report International Journal of Pediatric Endocrinology. 2013;2013(1): Regulation of Interferon-stimulated Gene (<italic>ISG</italic>)<italic>12</italic>, <italic>ISG15</italic>, and <italic>MX1</italic> and <italic>MX2</italic> by Conceptus Interferons (IFNTs) in Bovine Uterine Epithelial Cells Asian-Australasian Journal of Animal Sciences. 2013;26(6):795-803 SHOX gene in Leri-Weill syndrome and in idiopathic short stature Journal of Endocrinological Investigation. 2001;24(9):737-741 The Phenotype of Short Stature Homeobox Gene (SHOX) Deficiency in Childhood: Contrasting Children with Leri-Weill Dyschondrosteosis and Turner Syndrome The Journal of Pediatrics. 2005;147(4):499-507 The role of the SHOX gene in the pathophysiology of Turner syndrome Endocrinología y Nutrición. 2011;58(8):433-442 Detection of SHOX gene deletions in Egyptian children with idiopathic short stature using FISH Meta Gene. 2020;24:100697 |
