3M syndrome: Evaluating the clinical and laboratory features and the response of the growth hormone treatment: Single center experience-Reference-Cited by-同舟云学术

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3M syndrome: Evaluating the clinical and laboratory features and the response of the growth hormone treatment: Single center experience

Published:2023-10 Issue:10 Volume:66 Page:104828
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Karacan Küçükali Gülin^ORCID,Keskin Melikşah,Aycan Zehra,Savaş-Erdeve Şenay,Çetinkaya Semra

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference18 articles.

1. Use of the greulich-pyle "atlas of skeletal development of the hand and wrist" in a clinical context;Anderson;Am. J. Phys. Anthropol.,1971

2. Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination;Clayton;Clin. Endocrinol.,2012

3. 3-M syndrome: a novel CUL7 mutation associated with respiratory distress and a good response to GH therapy;Deeb;Endocrinol. Diabetes Metab. Case Rep.,2015

4. Severe short stature due to 3-M syndrome with a novel OBSL1 gene mutation;Demir;J. Pediatr. Endocrinol. Metab.,2013

5. Reference ranges for two automated chemiluminecent assays for serum insülin-like growth factor 1 (IGF-1) and IGF-binding protein 3 (IGFBP-3);Elmlinger;Clin. Chem. Lab. Med.,2004

Cited by 1 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

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