A duplicated gene in the breakpoint regions of the 7q11.23 Williams–Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK

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Human Molecular Genetics, Vol. 7, Iss. 3, 1998-03 ,pp. : 325-334

Oxford University Press

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Mechanisms of MLL gene rearrangement: site-specific DNA cleavage within the breakpoint cluster region is independent of chromosomal context

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Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2481-2491

Oxford University Press

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Identification of duplicated genes in 17q11.2 using FISH on stretched chromosomes and DNA fibers

By Bentivegna A.   Venturin M.   Gervasini C.   Corrado L.   Larizza L.   Riva P.  

Human Genetics, Vol. 109, Iss. 1, 2001-07 ,pp. : 48-54

Springer Publishing Company

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The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations

By Paulsson Kajsa   Haferlach Claudia   Fonatsch Christa   Hagemeijer Anne   Andersen Mette Klarskov   Slovak Marilyn L.   Johansson Bertil  

Human Molecular Genetics, Vol. 19, Iss. 8, 2010-04 ,pp. : 1507-1514

Oxford University Press

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Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2

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Human Molecular Genetics, Vol. 9, Iss. 4, 2000-03 ,pp. : 597-604

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