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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Necdin, a PraderWilli syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development

By Miller Nichol L.G.   Wevrick Rachel   Mellon Pamela L.  

Human Molecular Genetics, Vol. 18, Iss. 2, 2009-01 ,pp. : 248-260

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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Essential role for the Prader–Willi syndrome protein necdin in axonal outgrowth

By Lee Syann  

Human Molecular Genetics, Vol. 14, Iss. 5, 2005-03 ,pp. : 627-637

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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