Large genomic duplicons map to sites of instability in the Prader–Willi/Angelman syndrome chromosome region (15q11–q13)

By Christian Susan L.   Fantes Judy A.   Mewborn Stephanie K.   Huang Bing   Ledbetter David H.   Ledbetter D.H.   Nicholls R.D.   Jiang Y.   Webb T.   Pettigrew A.L.   Clayton-Smith J.   Repetto G.M.   Browne C.E.   Robinson W.P.   Schinzel A.A.   Long F.L.   Knoll J.H.   Kuwano A.   Mutirangura A.   Christian S.L.   Leana-Cox J.   Crolla J.A.   Huang B.   Wandstrat A.E.   Flejter W.L.   Cook E.H.   Donlon T.A.   Tantravahi U.   Buiting K.   Buiting K.   Ji Y.   Lehman A.L.   Nagase T.   Christian S.L.   Eichler E.E.   Yunis J.J.   Jauch A.   Luke S.   Wienberg J.   Sutcliffe J.S.   Kumar S.   Schuler G.D.   Kawasaki K.   Allikmets R.   Lupski J.   Cooper D.   Purandare S.M.   Lupski J.R.   Pentao L.   Reiter L.T.   Ballabio A.   Yen P.H.   Lakich D.   Bondeson M.L.   Small K.   Small K.   Lewis S.M.   Konrad M.   Lehrman M.A.   Carrozzo R.   Chen K.S.   Lowery M.C.   Nickerson E.   Budarf M.L.   Osbourne L.R.   Perez Jurado L.A.   Perez Jurado L.A.   Morrow B.   Edelmann L.   McTaggert K.E.   Tomlinson I.M.   Nagaoka H.   Purandare S.M.   Regnier V.   Kehrer-Sawatzki H.   Ritchie R.J.   Chong S.S.   Finelli P.   Trask B.J.   van den Engh G.  

Human Molecular Genetics, Vol. 8, Iss. 6, 1999-06 ,pp. : 1025-1037

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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Imprinted Segments in the Human Genome: Different Dna Methylation Patterns in the Prader-Willi/Angelman Syndrome Region As Determined by the Genomic Sequencing Method

By Zeschnigk Michael   Schmitz Birgit   Dittrich Bärbel   Buiting Karin   Horsthemke Bernhard   Doerfler Walter  

Human Molecular Genetics, Vol. 6, Iss. 3, 1997-01 ,pp. : 387-395

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Establishing the epigenetic status of the Prader–Willi/Angelman imprinting center in the gametes and embryo

By Kantor Boris   Kaufman Yotam   Makedonski Kirill   Shemer Ruth  

Human Molecular Genetics, Vol. 13, Iss. 22, 2004-11 ,pp. : 2767-2779

Oxford University Press

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Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader–Willi/Angelman syndrome region

By Cavaillé J.  

Human Molecular Genetics, Vol. 11, Iss. 13, 2002-06 ,pp. : 1527-1538

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