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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2013 | 2 |
2014 | 2 |
2015 | 2 |
2016 | 1 |
2024 | 0 |
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5 results
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Page 1
Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature.
Genet Med. 2015 Feb;17(2):149-57. doi: 10.1038/gim.2014.83. Epub 2014 Jul 31.
Genet Med. 2015.
PMID: 25077648
Free PMC article.
Review.
Compound heterozygous microdeletion of chromosome 15q13.3 region in a child with hypotonia, impaired vision, and global developmental delay.
Prasun P, Hankerd M, Kristofice M, Scussel L, Sivaswamy L, Ebrahim S.
Prasun P, et al.
Am J Med Genet A. 2014 Jul;164A(7):1815-20. doi: 10.1002/ajmg.a.36535. Epub 2014 Apr 3.
Am J Med Genet A. 2014.
PMID: 24700535
Review.
Item in Clipboard
The 15q13.3 deletion syndrome: Deficient α(7)-containing nicotinic acetylcholine receptor-mediated neurotransmission in the pathogenesis of neurodevelopmental disorders.
Deutsch SI, Burket JA, Benson AD, Urbano MR.
Deutsch SI, et al.
Prog Neuropsychopharmacol Biol Psychiatry. 2016 Jan 4;64:109-17. doi: 10.1016/j.pnpbp.2015.08.001. Epub 2015 Aug 7.
Prog Neuropsychopharmacol Biol Psychiatry. 2016.
PMID: 26257138
Review.
Item in Clipboard
Dosage-sensitivity of imprinted genes expressed in the brain: 15q11-q13 and neuropsychiatric illness.
McNamara GI, Isles AR.
McNamara GI, et al.
Biochem Soc Trans. 2013 Jun;41(3):721-6. doi: 10.1042/BST20130008.
Biochem Soc Trans. 2013.
PMID: 23697931
Review.
Item in Clipboard
Copy number variants are frequent in genetic generalized epilepsy with intellectual disability.
Mullen SA, Carvill GL, Bellows S, Bayly MA, Trucks H, Lal D, Sander T, Berkovic SF, Dibbens LM, Scheffer IE, Mefford HC.
Mullen SA, et al.
Neurology. 2013 Oct 22;81(17):1507-14. doi: 10.1212/WNL.0b013e3182a95829. Epub 2013 Sep 25.
Neurology. 2013.
PMID: 24068782
Free PMC article.
Review.
Item in Clipboard
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