Smallest terminal deletion of the long arm of chromosome 2 in a mildly affected boy
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference5 articles.
1. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37)
2. Rapid detection of human chromosome 21 aberrations by in situ hybridization.
3. A case of deletion 2q35----qter and a peculiar phenotype.
4. Deletion 2q: two new cases with karyotypes 46,XY,del(2)(q31q33) and 46,XX,del(2)(q36).
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1. A rare case of 2q37 deletion syndrome presented with patent foramen ovale;Clinical Case Reports;2023-11
2. Genotype and phenotype correlation in 103 individuals with 2q37 deletion syndrome reveals incomplete penetrance and supports HDAC4 as the primary genetic contributor;American Journal of Medical Genetics Part A;2019-03-07
3. Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly;Taiwanese Journal of Obstetrics and Gynecology;2012-06
4. Deletion 2q37: An Identifiable Clinical Syndrome With Mental Retardation and Autism;Journal of Child Neurology;2008-07
5. Clinical phenotype associated with terminal 2q37 deletion;Clinical Genetics;2008-06-28
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