Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients-Reference-Cited by-同舟云学术

Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients

Published:2015-04-09 Issue:1 Volume:8 Page:
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Choucair Nancy,Ghoch Joelle Abou,Corbani Sandra,Cacciagli Pierre,Mignon-Ravix Cecile,Salem Nabiha,Jalkh Nadine,El Sabbagh Sandra,Fawaz Ali,Ibrahim Tony,Villard Laurent,Mégarbané André,Chouery Eliane

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry, medical,Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Link

http://link.springer.com/content/pdf/10.1186/s13039-015-0130-y.pdf

Reference48 articles.

1. Schalock RL, Borthwick-Duffy SA, Bradley VJ, Buntinx WHE, Coulter DL, Craig EM, et al. Intellectual disability: definition, classification, and systems of supports. 11th ed. American Association on Intellectual and Developmental Disabilities; 2010.

2. OMS | Chapitre 2: Impact des troubles mentaux et du comportement http://www.who.int/whr/2001/chapter2/fr/index4.html

3. Roeleveld N, Zielhuis GA, Gabreëls F. The prevalence of mental retardation: a critical review of recent literature. Dev Med Child Neurol. 1997;39:125–32.

4. Rauch A, Hoyer J, Guth S, Zweier C, Kraus C, Becker C, et al. Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation. Am J Med Genet A. 2006;140:2063–74.

5. Scior K. Public awareness, attitudes and beliefs regarding intellectual disability: a systematic review. Res Dev Disabil. 2011;32:2164–82.

Cited by 6 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. 15q26.3 deletions distal to IGF1R cause growth retardation, congenital heart defect and skeletal anomalies: Case report and review of literature;American Journal of Medical Genetics Part A;2023-07-12

2. Pirenperone relieves the symptoms of fragile X syndrome in Fmr1 knockout mice;2022-08-11

3. Long contiguous stretches of homozygosity detected by chromosomal microarrays (CMA) in patients with neurodevelopmental disorders in the South of Brazil;BMC Medical Genomics;2019-03-12

4. Abordaje citogenético y citogenómico de pacientes con discapacidad intelectual y malformaciones congénitas;Acta Pediátrica de México;2017-11-13

5. Copy number variation analysis of patients with intellectual disability from North-West Spain;Gene;2017-08