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, fragile site, aphidicolin type, common, fra(7)(q21.2)
National Institutes of Health
Semantic Scholar uses AI to extract papers important to this topic.
Human chromosome fragility.
Biochimica et biophysica acta
Corpus ID: 19612490
Fragile sites are heritable specific chromosome loci that exhibit an increased frequency of gaps, poor staining, constrictions or…
Clinico-pathological significance of cell-type-specific loss of heterozygosity on chromosome 7q21: analysis of 318 microdissected thyroid lesions.
Corpus ID: 25418250
A careful pathological examination often reveals the presence of different lesions at various stages of tumor progression and…
Molecular Basis for Expression of Common and Rare Fragile Sites
Molecular and Cellular Biology
Corpus ID: 13106097
ABSTRACT Fragile sites are specific loci that form gaps, constrictions, and breaks on chromosomes exposed to partial replication…
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