Genotypes and Phenotypes of Children with SHOX Deficiency in France-Reference-Cited by-同舟云学术

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Genotypes and Phenotypes of Children with SHOX Deficiency in France

Published:2012-07 Issue:7 Volume:97 Page:E1257-E1265
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Rosilio Myriam,Huber-Lequesne Céline,Sapin Hélène,Carel Jean-Claude,Blum Werner F.,Cormier-Daire Valérie

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 54 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. Identification of a second genetic alteration in patients withSHOXdeficiency individuals: a potential explanation for phenotype variability;European Journal of Endocrinology;2023-09-01

2. Leri–Weill Dyschondrosteosis Caused by a Leaky Homozygous SHOX Splice-Site Variant;Genes;2023-04-07

3. Genetic Analysis and Sonography Characteristics in Fetus with SHOX Haploinsufficiency;Genes;2023-01-04

4. Detection of Del/Dup Inside SHOX/PAR1 Region in Children and Young Adults with Idiopathic Short Stature;Genes;2021-09-29

5. Identification and Tissue-Specific Characterization of Novel SHOX-Regulated Genes in Zebrafish Highlights SOX Family Members Among Other Genes;Frontiers in Genetics;2021-05-27

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