Microarray comparative genomic hybridization and FISH studies of an unbalanced cryptic telomeric 2p deletion/16q duplication in a patient with mental retardation and behavioral problems
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference11 articles.
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1. Molecular cytogenetic characterization of partial monosomy�2p and trisomy 16q in a newborn: A case report;Experimental and Therapeutic Medicine;2019-06-20
2. Clinical and molecular findings in 39 patients with KBG syndrome caused by deletion or mutation ofANKRD11;American Journal of Medical Genetics Part A;2016-09-08
3. Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity;Genetics in Medicine;2015-06
4. Early-onset obesity and paternal 2pter deletion encompassing the ACP1, TMEM18, and MYT1L genes;European Journal of Human Genetics;2013-10-16
5. Molecular cytogenetic characterization of 2p23.2p23.3 deletion in a child with developmental delay, hypotonia and cryptorchism;European Journal of Medical Genetics;2013-01
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