Prenatal diagnosis of 20p13 microdeletion syndrome
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference13 articles.
1. Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes;Lupski;PLoS Genet,2005
2. SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay;An;Am J Med Genet B Neuropsychiatr Genet,2013
3. A tale of two deletions: a report of two novel 20p13-> pter deletions;McGill;Am J Med Genet,2010
4. SOX22 is a new member of the SOX gene family, mainly expressed in human nervous tissue;Jay;Hum Mol Genet,1997
5. Molecular characterization of a transport vesicle protein Neurensin-2, a homologue of Neurensin-1, expressed in neural cells;Nakanishi;Brain Res,2006
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