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FGFR2 Amplification in Colorectal Adenocarcinoma

FGFR2 is recurrently amplified in 5% of gastric cancers and 1-4% of breast cancers; however, this molecular alteration has never been reported in a pr...

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Method for the molecular cytogenetic visualization of fragile site FRAXA

Fragile X syndrome is one of the most common reasons for human hereditary mental retardation. It is associated with the expansion of CGG repeats in th...

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t(6;11)(p21;q12)/TFEB gene fusion-associated renal cell carcinoma: a case report and review of literature

t(6;11)(p21;q12)/TFEB gene fusion-associated renal cell carcinoma is a recently recognized renal cell carcinoma caused by the formation of Alpha-TFEB ...

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