Association of acetylated histones with paternally expressed genes in the Prader–Willi deletion region

By B.Fulmer-Smentek S.   Francke U.  

Human Molecular Genetics, Vol. 10, Iss. 6, 2001-03 ,pp. : 645-652

Oxford University Press

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The Necdin Gene is Deleted in Prader-Willi Syndrome and is Imprinted in Human and Mouse

By MacDonald Heather R.   Wevrick Rachel  

Human Molecular Genetics, Vol. 6, Iss. 11, 1997-10 ,pp. : 1873-1878

Oxford University Press

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Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader–Willi syndrome genetic region

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Human Molecular Genetics, Vol. 8, Iss. 5, 1999-05 ,pp. : 795-803

Oxford University Press

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Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader–Willi syndrome

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Human Molecular Genetics, Vol. 9, Iss. 20, 2000-12 ,pp. : 3101-3110

Oxford University Press

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An Imprinted Mouse Transcript Homologous to the Human Imprinted in Prader-Willi Syndrome ( IPW ) Gene

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Human Molecular Genetics, Vol. 6, Iss. 2, 1997-01 ,pp. : 325-332

Oxford University Press

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