An imprinted antisense transcript at the human GNAS1 locus

By Hayward Bruce E.   Bonthron David T.  

Human Molecular Genetics, Vol. 9, Iss. 5, 2000-03 ,pp. : 835-841

Oxford University Press

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Identification and characterization of an imprinted antisense RNA ( MESTIT1 ) in the human MEST locus on chromosome 7q32

By Nakabayashi Kazuhiko  

Human Molecular Genetics, Vol. 11, Iss. 15, 2002-07 ,pp. : 1743-1756

Oxford University Press

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Pathophysiological Mechanisms of Dominant and Recessive KvLQT1 K+ Channel Mutations Found in Inherited Cardiac Arrhythmias

By Wollnik Bernd  

Human Molecular Genetics, Vol. 6, Iss. 11, 1997-10 ,pp. : 1943-1949

Oxford University Press

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IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome

By Tyson Jessica  

Human Molecular Genetics, Vol. 6, Iss. 12, 1997-11 ,pp. : 2179-2185

Oxford University Press

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Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith–Wiedemann syndrome

By Horike Shin-ichi   Mitsuya Kohzoh   Meguro Makiko   Kotobuki Noriko   Kashiwagi Akiko   Notsu Tomomi   Schulz ThomasC.   Shirayoshi Yasuaki   Oshimura Mitsuo  

Human Molecular Genetics, Vol. 9, Iss. 14, 2000-09 ,pp. : 2075-2083

Oxford University Press

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