Clinical utility gene card for: 15q13.3 microdeletion syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/ejhg201488.pdf
Reference53 articles.
1. Makoff AJ, Flomen RH : Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromes. Genome Biol 2007; 8: R114.
2. Sharp AJ, Mefford HC, Li K et al: A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures. Nat Genet 2008; 40: 322–328.
3. Stefansson H, Rujescu D, Cichon S et al: Large recurrent microdeletions associated with schizophrenia. Nature 2008; 455: 232–236.
4. International Schizophrenia Consortium: Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 2008; 455: 237–241.
5. Miller DT, Shen Y, Weiss LA et al: Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders. J Med Genet 2009; 46: 242–248.
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4. Brain Network Analysis of EEG Recordings Can Be Used to Assess Cognitive Function in Teenagers With 15q13.3 Microdeletion Syndrome;Frontiers in Neuroscience;2021-01-28
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