A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader–Willi syndrome critical region

By Jong M.T.C.  

Human Molecular Genetics, Vol. 8, Iss. 5, 1999-05 ,pp. : 783-793

Oxford University Press

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

By Wevrick Rachel   Francke Uta  

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

Oxford University Press

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The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader–Willi region

By Boccaccio Irène   Glatt-Deeley Heather   Watrin Françoise   Roëckel Nathalie   Lalande Marc   Muscatelli Françoise  

Human Molecular Genetics, Vol. 8, Iss. 13, 1999-12 ,pp. : 2497-2505

Oxford University Press

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Expression and imprinting of MAGEL2 suggest a role in Prader–Willi syndrome and the homologous murine imprinting phenotype

By Lee Syann   Kozlov Serguei  

Human Molecular Genetics, Vol. 9, Iss. 12, 2000-07 ,pp. : 1813-1819

Oxford University Press

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Large-scale evaluation of imprinting status in the Prader–Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes

By Oshimura M.  

Human Molecular Genetics, Vol. 10, Iss. 4, 2001-02 ,pp. : 383-394

Oxford University Press

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