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BlankDetection of risk-identifying chromosomal abnormalities and genomic

profiling by multiplex ligation-dependent probe amplification in chronic

lymphocytic leukemia.

A Buijs, PJ Krijtenburg, and E Meijer

Haematologica, October 1, 2006; 91(10): 1434-5.

Division of Biomedical Genetics, Department of Medical Genetics,

University Medical Center Utrecht, PO BOX 85090, 3508 AB Utrecht, The

Netherlands. a.buijs@....

We performed genomic profiling using multiplex ligation-dependent probe

amplification (MLPA) in 54 cases with suspected or advanced chronic lymphocytic

leukemia (CLL). MLPA detected abnormalities when the percentage of mutated cells

was greater than ~35%. Loss of 9p21 CDNK2A/B was revealed. MLPA is an

economically attractive, powerful tool in trial-based, centralized

risk-assessment for CLL.

PMID: 17018399

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