Phenotype of a child with Angelman syndrome born to a woman with Prader–Willi syndrome

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 9, 2015-09 ,pp. : 2138-2144

John Wiley & Sons Inc

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

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

By Lee Syann  

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Oxford University Press

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Autism spectrum disorder in Prader–Willi syndrome: A systematic review

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John Wiley & Sons Inc

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