SHOX: Growth, Léri–Weill and Turner Syndromes
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference41 articles.
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1. Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency;Annals of Pediatric Endocrinology & Metabolism;2024-06-30
2. Shortened fetal long bones: A notable intrauterine phenotypic feature in SHOX‐associated skeletal dysplasia;Prenatal Diagnosis;2023-08
3. A novel preimplantation genetic testing strategy for a subtelomeric genetic disorder: A case study;Genes & Diseases;2023-07
4. Genetic analysis of Turner syndrome in Tunisian patients;Journal of The Arab Society for Medical Research;2023-01
5. Detection of Turner syndrome using hand X-ray using anchor based links segmentation method;Proceedings of the Institution of Mechanical Engineers, Part H: Journal of Engineering in Medicine;2022-02-04
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