Description and genetic mapping of Polypodia : an X-linked dominant mouse mutant with ectopic caudal limbs and other malformations

By Lehoczky Jessica   Cai Wei-Wen   Douglas Julie   Moran Jennifer   Beier David   Innis Jeffrey  

Mammalian Genome, Vol. 17, Iss. 9, 2006-09 ,pp. : 903-913

Springer Publishing Company

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OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance

By Pesch U.E.A.  

Human Molecular Genetics, Vol. 10, Iss. 13, 2001-06 ,pp. : 1359-1368

Oxford University Press

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Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant EmeryDreifuss muscular dystrophy

By Muchir Antoine   Pavlidis Paul   Bonne Gisle   Hayashi Yukiko K.   Worman Howard J.  

Human Molecular Genetics, Vol. 16, Iss. 15, 2007-08 ,pp. : 1884-1895

Oxford University Press

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A new locus for X-linked dominant Charcot–Marie–Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 ( PDK3 ) gene

By Kennerson Marina L.   Yiu Eppie M.   Chuang David T.   Kidambi Aditi   Tso Shih-Chia   Ly Carolyn   Chaudhry Rabia   Drew Alexander P.   Rance Gary   Delatycki Martin B.   Züchner Stephan   Ryan Monique M.   Nicholson Garth A.  

Human Molecular Genetics, Vol. 22, Iss. 7, 2013-04 ,pp. : 1404-1416

Oxford University Press

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Mutations in the RPGR gene cause X-linked cone dystrophy

By Yang Z.  

Human Molecular Genetics, Vol. 11, Iss. 5, 2002-03 ,pp. : 605-611

Oxford University Press

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