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

Access to resources Recommend Favorite

DFNB44, a Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus, Maps to Chromosome 7p14.1-q11.22

By  

Human Heredity, Vol. 57, Iss. 4, 2004-11 ,pp. : 195-199

Karger

Access to resources Recommend Favorite

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects

By Morton C.C.  

Human Molecular Genetics, Vol. 8, Iss. 2, 1999-02 ,pp. : 361-366

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

By Griffin A.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2509-2514

Oxford University Press

Access to resources Recommend Favorite