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. 2014 Nov;22(11):1338.
doi: 10.1038/ejhg.2014.88. Epub 2014 May 14.

Clinical utility gene card for: 15q13.3 microdeletion syndrome

Maria Tropeano  1 , Joris Andrieux  2 , Evangelos Vassos  1 , David A Collier  3
Affiliations

Clinical utility gene card for: 15q13.3 microdeletion syndrome

Maria Tropeano et al. Eur J Hum Genet. 2014 Nov.
No abstract available

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References

    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. - PMC - PubMed
    1. 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. - PMC - PubMed
    1. Stefansson H, Rujescu D, Cichon S, et al. Large recurrent microdeletions associated with schizophrenia. Nature. 2008;455:232–236. - PMC - PubMed
    1. International Schizophrenia Consortium Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature. 2008;455:237–241. - PMC - PubMed
    1. 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. - PMC - PubMed

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