A patient with a ring chromosome 2 and microdeletion of 2q detected using FISH: Further support for ?ring chromosome 2 syndrome?
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference17 articles.
1. Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes
2. Effective monosomy or trisomy of chromosome band 2q37.3 due to the unbalanced segregation of a 2;11 translocation
3. Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype
4. Clinical phenotype associated with terminal 2q37 deletion
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1. Ring Chromosome 2;Human Ring Chromosomes;2024
2. Clinico-radiological and molecular characterization of a child with ring chromosome 2 presenting growth failure, microcephaly, kidney and brain malformations;Molecular Cytogenetics;2015-03-05
3. 35-Year Follow-Up of a Case of Ring Chromosome 2: Array-CGH Analysis and Literature Review of the Ring Syndrome;Cytogenetic and Genome Research;2015
4. Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization;Gene;2013-04
5. A genome-wide scan for genes involved in primary vesicoureteric reflux;Journal of Medical Genetics;2007-08-23
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