A new case of interstitial 6q16.2 deletion in a patient with Prader–Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity-Reference-Cited by-同舟云学术

A new case of interstitial 6q16.2 deletion in a patient with Prader–Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity

Published:2006-07 Issue:4 Volume:49 Page:298-305
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Varela Monica C.,Simões-Sato Alex Y.,Kim Chong A.,Bertola Débora R.,De Castro Claudia I.E.,Koiffmann Celia P.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference23 articles.

1. Two Cases of maternal uniparental disomy 14 with a phenotype overlapping with the Prader–Willi phenotype;Berends;Am. J. Med. Genet.,1999

2. Cloning of two human homologs of the Drosophila single-minded gene SIM1 on chromosome 6q and SIM2 on 21q within the Down syndrome chromosomal region;Chrast;Genome Res.,1997

3. Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?;Cormier-Daire;J. Med. Genet.,2003

4. Fat chance: genetic syndromes with obesity;Delrue;Clin. Genet.,2004

5. Mosaicism for deletion 1p36.33 in a patient with obesity and hyperphagia;Eugster;Am. J. Med. Genet.,1997

Cited by 46 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. Rare genetic forms of obesity in childhood and adolescence, a comprehensive review of their molecular mechanisms and diagnostic approach;European Journal of Pediatrics;2023-08-23

2. Research Article Genotypic and phenotypic relationship between Prader-Willi and Prader-Willi-Like syndromes;Genetics and Molecular Research;2023

3. Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China;Orphanet Journal of Rare Diseases;2022-06-13

4. Syndromic obesity with neurodevelopmental delay: Opportunities for targeted interventions;European Journal of Medical Genetics;2022-03

5. The Spectrum of the Prader–Willi-like Pheno- and Genotype: A Review of the Literature;Endocrine Reviews;2021-08-30