Concepedia

Mark Houseman

MH

Statistics

Publications

7

Citations

911

H-Index

7

Active since

1997

Affiliations

St James's University Hospital(Current)

Royal Children's Hospital

University of Manchester

University of Leeds

Mark Houseman is an author at St James's University Hospital specializing in genetics, medical genetics, and molecular genetics.

Publications per year

1997–2001

7

Publications

7

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 · 636 citations · Full text

, , +11

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

, , +15

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

, , +17

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

, , +14

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

, , +11

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