Chromosome 2q37 deletion: Clinical and molecular aspects
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference66 articles.
1. Subtelomere deletions and translocations are frequently familial
2. Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes
3. A patient with a ring chromosome 2 and microdeletion of 2q detected using FISH: Further support for ?ring chromosome 2 syndrome?
4. Subtelomeric rearrangements detected in patients with idiopathic mental retardation
5. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes
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2. A rare case of 2q37 deletion syndrome presented with patent foramen ovale;Clinical Case Reports;2023-11
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