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Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells
PaperCitations, authors & open-access status
Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 273 citations, 2000 year and bronze oa status.
273
Citations
2000
Year
bronze
OA Status