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Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: An update and literature review

1 Jan 2001

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PMID: 11339380
DOI: 10.1097/00125817-200101000-00003

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: An update and literature reviewPMID 11339380Read ↗

22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated FeaturesSemantic proximity Read ↗

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Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins.Semantic proximity Read ↗

Inverted low-copy repeats and genome instability--a genome-wide analysis.Semantic proximity Read ↗

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Deletion 22q11: Spectrum of Associated DisordersSemantic proximity Read ↗

Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype–Phenotype CorrelationSemantic proximity Read ↗

Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2.Semantic proximity Read ↗

Population differences of chromosome 22q11.2 duplication structure predispose differentially to microdeletion and inversionSemantic proximity Read ↗

NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits.Semantic proximity Read ↗

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