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

By Jong M.T.C.  

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

Oxford University Press

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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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Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader–Willi syndrome

By Tsai Ting-Fen   Jiang Yong-hui   Bressler Jan   Armstrong Dawna   Beaudet Arthur L.   Jiang Y.   Lalande M.   Nicholls R.D.   Malzac P.   Fang P.   Cassidy S.B.   Saitoh S.   Leff S.E.   Özçelik T.   Cattanach B.M.   Yang T.   McAllister G.   Schmauss C.   Sun Y.   Kuslich C.D.   Schulze A.   Conroy J.M.   Gabriel J.M.   Glenn C.C.   Shemer R.   Sutcliffe J.S.   Zeschnigk M.   Ramirez-Solis R.   Jiang Y.-H.   Watrin F.   Albrecht U.   Johnson D.K.   McMahon A.P.   Ramirez-Solis R.   Ramirez-Solis R.   Sambrook J.   Wevrick R.   Wagstaff J.  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1357-1364

Oxford University Press

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