3M Syndrome: A Report of Four Cases in Two Families
Author:
Publisher
Galenos Yayinevi
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health
Link
http://cms.galenos.com.tr/FileIssue/1/380/article/154-159.pdf
Cited by 15 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. Clinical and Molecular Spectrum Along With Genotype-Phenotype Correlation of 25 Patients Diagnosed With 3M Syndrome: A Study from Turkey;2024-08-19
2. Clinical profiles and molecular genetic analyses of 98 Chinese children with short statures;Frontiers in Genetics;2024-06-12
3. 3M syndrome: Evaluating the clinical and laboratory features and the response of the growth hormone treatment: Single center experience;European Journal of Medical Genetics;2023-10
4. Structural and functional insights into a novel homozygous missense pathogenic variant in CUL7 identified in consanguineous Pakistani family;Journal of Biomolecular Structure and Dynamics;2023-06-22
5. 3-M syndrome – a primordial short stature disorder with novel CUL7 mutation in two Indian patients;Journal of Pediatric Endocrinology and Metabolism;2021-10-22
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