Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31

By Coffeen Christin M.  

Human Molecular Genetics, Vol. 9, Iss. 5, 2000-03 ,pp. : 787-793

Oxford University Press

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A Gene for Non-Syndromic Autosomal Dominant Progressive Postlingual Sensorineural Hearing Loss Maps to Chromosome 14q12–13

By Manolis Evangelos N.  

Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 1047-1050

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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Chromosome 1 localization of a gene for autosomal dominant medullary cystic kidney disease (ADMCKD)

By Christodoulou K.  

Human Molecular Genetics, Vol. 7, Iss. 5, 1998-05 ,pp. : 905-911

Oxford University Press

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Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23

By Kannabiran Chitra   Singh Hardeep   Jalali Subhadra  

Human Genetics, Vol. 131, Iss. 5, 2012-05 ,pp. : 717-723

Springer Publishing Company

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