15q26.1 microdeletion encompassing only CHD2 and RGMA in two adults with moderate intellectual disability, epilepsy and truncal obesity
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference12 articles.
1. Deletion of the RGMA and CHD2 genes in a child with epilepsy and mental deficiency;Capelli;Eur J Med Genet,2012
2. Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1;Carvill;Nat Genet,2013
3. Microdeletion of chromosome 15q26.1 in a child with intractable generalized epilepsy;Dhamija;Pediatr Neurol,2011
4. Inactivation of Ras by p120GAP via focal adhesion kinase dephosphorylation mediates RGMa-induced growth cone collapse;Endo;J Neurosci,2009
5. Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: two patients and review of the literature;Klaassens;Am J Med Genet A,2007
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