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[Sixty-seven percent of GBs (91/136) and 21% of AAs (8/39) had abnormalities of the G1-S control system either by mutation/homozygous deletion of RB1, CDKN2A or CDKN2B, or amplification of CDK4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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