The idic(15) syndrome: Expanding the phenotype
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35366/fullpdf
Reference11 articles.
1. The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder;Battaglia;Brain Dev,2005
2. The inv dup (15) or idic (15) syndrome (Tetrasomy 15q);Battaglia;Orphanet J Rare Dis,2008
3. The behavioral phenotype of the idic(15) syndrome;Battaglia;Am J Med Genet C Semin Med Genet,2010
4. The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13;Hogart;Neurobiol Dis,2010
5. Phenotypic spectrum of 20 novel patients with molecularly defined supernumerary marker chromosomes 15 and a review of the literature;Kleefstra;Am J Med Genet Part A,2010
Cited by 3 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. Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature;Molecular Cytogenetics;2018-02-05
2. Neurological features and long-term follow-up in 15q11.2-13.1 duplication;European Journal of Medical Genetics;2013-11
3. Paradoxical worsening of seizure activity with pregabalin in an adult with isodicentric 15 (IDIC-15) syndrome involving duplications of the GABRB3, GABRA5 and GABRG3 genes;BMC Neurology;2013-05-10
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