Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites.

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Bibliographic Details
Title: Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites.
Authors: Burrow AA; Department of Biochemistry, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1016, USA. aburrow@wfubmc.edu, Williams LE, Pierce LC, Wang YH
Source: BMC genomics [BMC Genomics] 2009 Jan 30; Vol. 10, pp. 59. Date of Electronic Publication: 2009 Jan 30.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 100965258 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2164 (Electronic) Linking ISSN: 14712164 NLM ISO Abbreviation: BMC Genomics Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1471-2164
DOI:10.1186/1471-2164-10-59