Interstitial deletion 2q31→q33
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference9 articles.
1. Interstitial deletion of the long arm of chromosome 2 in a polymalformed newborn-karyotype: 46,XX,del(2)(q21;q24)
2. MN Blood-Group Locus: Data Concerning the Possible Chromosomal Location
3. Mapping Human Autosomes: Assignment of the MN Locus to a Specific Segment in the Long Arm of Chromosome No. 2
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2. Left ventricular outflow tract obstruction: should cardiac screening be offered to first-degree relatives?;Heart;2011-02-22
3. Genotype-phenotype correlation in eight new patients with a deletion encompassing 2q31.1;American Journal of Medical Genetics Part A;2010-05
4. Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome;PLoS ONE;2009-08-10
5. Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: An array-based genotype–phenotype correlation and a comprehensive review of previously published cases;Epilepsy Research;2008-09
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