Author:
Anazi S,Maddirevula S,Faqeih E,Alsedairy H,Alzahrani F,Shamseldin H E,Patel N,Hashem M,Ibrahim N,Abdulwahab F,Ewida N,Alsaif H S,Al sharif H,Alamoudi W,Kentab A,Bashiri F A,Alnaser M,AlWadei A H,Alfadhel M,Eyaid W,Hashem A,Al Asmari A,Saleh M M,AlSaman A,Alhasan K A,Alsughayir M,Al Shammari M,Mahmoud A,Al-Hassnan Z N,Al-Husain M,Osama Khalil R,Abd El.Meguid N,Masri A,Ali R,Ben-Omran T,El.Fishway P,Hashish A,Ercan Sencicek A,State M,Alazami A M,Salih M A,Altassan N,Arold S T,Abouelhoda M,Wakil S M,Monies D,Shaheen R,Alkuraya F S
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Psychiatry and Mental health,Molecular Biology
Reference49 articles.
1. Maulik PK, Harbour CK . Epidemiology of intellectual disability. In: JH Stone, M Blouin (eds). International Encyclopedia of Rehabilitation 2010. Available at: http://cirrie.buffalo.edu/encyclopedia/en/article/144/.
2. Association AP Diagnostic and Statistical Manual of Mental Disorders (DSM-5®). American Psychiatric Pub 2013.
3. Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP et al. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet 2010; 86: 749–764.
4. Männik K, Mägi R, Macé A, Cole B, Guyatt AL, Shihab HA et al. Copy number variations and cognitive phenotypes in unselected populations. JAMA 2015; 313: 2044–2054.
5. Rauch A, Wieczorek D, Graf E, Wieland T, Endele S, Schwarzmayr T et al. Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. Lancet 2012; 380: 1674–1682.