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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The human centromeric survival motor neuron gene ( SMN2 ) rescues embryonic lethality in Smn –/– mice and results in a mouse with spinal muscular atrophy

By Monani Umrao R.  

Human Molecular Genetics, Vol. 9, Iss. 3, 2000-02 ,pp. : 333-339

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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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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Distant cis -elements regulate imprinted expression of the mouse p57 Kip2 ( Cdkn1c ) gene: implications for the human disorder, Beckwith–Wiedemann syndrome

By John R.M.   Ainscough J.F.   Barton S.C.   Surani M.A.  

Human Molecular Genetics, Vol. 10, Iss. 15, 2001-07 ,pp. : 1601-1609

Oxford University Press

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