Expression of a truncated Sall1 transcriptional repressor is responsible for Townes–Brocks syndrome birth defects

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Human Molecular Genetics, Vol. 12, Iss. 17, 2003-09 ,pp. : 2221-2227

Oxford University Press

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CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome

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Human Molecular Genetics, Vol. 19, Iss. 14, 2010-07 ,pp. : 2858-2866

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Association and regulation of the BLM helicase by the telomere proteins TRF1 and TRF2

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Human Molecular Genetics, Vol. 13, Iss. 17, 2004-09 ,pp. : 1919-1932

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Wolfram syndrome 1 gene ( WFS1 ) product localizes to secretory granules and determines granule acidification in pancreatic -cells

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Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1274-1284

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Poly(ADP-ribose) polymerase 2 localizes to mammalian active centromeres and interacts with PARP-1, Cenpa, Cenpb and Bub3, but not Cenpc

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Human Molecular Genetics, Vol. 11, Iss. 19, 2002-07 ,pp. : 2319-2329

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