A Gene for a Dominant Form of Non-Syndromic Sensorineural Deafness ( DFNA11 ) Maps Within the Region Containing the DFNB2 Recessive Deafness Gene

By Tamagawa Yuya   Kitamura Ken   Ishida Takashi   Ishikawa Kazuhiro   Tanaka Hajime   Tsuji Shoji   Nishizawa Masatoyo  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 849-852

Oxford University Press

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Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 12, 2015-12 ,pp. : 3054-3061

John Wiley & Sons Inc

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Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy

By Winkelmann Juliane   Lin Ling   Schormair Barbara   Kornum Birgitte R.   Faraco Juliette   Plazzi Giuseppe   Melberg Atle   Cornelio Ferdinando   Urban Alexander E.   Pizza Fabio   Poli Francesca   Grubert Fabian   Wieland Thomas   Graf Elisabeth   Hallmayer Joachim   Strom Tim M.   Mignot Emmanuel  

Human Molecular Genetics, Vol. 21, Iss. 10, 2012-05 ,pp. : 2205-2210

Oxford University Press

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The Gene Responsible for Autosomal Dominant Doyne's Honeycomb Retinal Dystrophy ( DHRD ) Maps to Chromosome 2p16

By Gregory Cheryl Y.  

Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 1055-1059

Oxford University Press

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A Gene for Autosomal Dominant Late-Onset Progressive Non-Syndromic Hearing Loss, DFNA10 , Maps to Chromosome 6

By O'Neill Marsha E.   Marietta Jacquie   Nishimura Darryl   Wayne Sigrid   Van Camp Guy   Van Laer Lut   Negrini Clelia   Wilcox Edward R.   Chen Achih   Fukushima Kunihiro   Ni Li   Sheffield Val C.   Smith Richard J. H.  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 853-856

Oxford University Press

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