Mark Houseman

Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

Françoise Denoyelle, Dominique Weil, Marion A. Maw et al. · Human Molecular Genetics · 1997 · 635 citations · Full text

Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss

Mark Houseman, Lucy Ellis, Alistair T. Pagnamenta et al. · Journal of Medical Genetics · 2001 · 84 citations · Full text

A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.

David A. Campbell, Duncan P. McHale, Kathryn Brown et al. · Journal of Medical Genetics · 1997 · 57 citations · Full text

Sensorineural Hearing Loss, Genetics, Inherited Deafness +24

Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations — molecular and audiological findings

R F Mueller, A Nehammer, Anna Middleton et al. · International Journal of Pediatric Otorhinolaryngology · 1999 · 57 citations

Auditory Processing, Developmental Biology, Audiological Findings +12

A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23–q31

Lj Pulleyn, Emma Roberts, A Carridice et al. · European Journal of Human Genetics · 2000 · 28 citations · Full text

Auditory Processing, Chromosome 2Q23–q31, Health Sciences +13