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A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

Data up to Jan 2025

Published1997
Citations60
References18

Total Citations Per Year

Abstract

References (18)

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1996 • 2,983 citations

Easy calculations of lod scores and genetic risks on small computers.

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Faster sequential genetic linkage computations.

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1995 • 421 citations

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1995 • 374 citations

Human/Mouse Homology Relationships

1996 • 373 citations

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1995 • 301 citations

Localization of two genes for usher syndrome type I to chromosome 11

1992 • 221 citations

Autosomal Recessive Non-Syndromic Deafness Locus (DFNB8) Maps on Chromosome 21Q22 in a Large Consanguineous Kindred from Pakistan

1996 • 138 citations

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene

1994 • 133 citations

A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene

1996 • 91 citations

A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval

1994 • 85 citations

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1993 • 40 citations

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1993 • 36 citations

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1995 • 36 citations

Assignment of the Human Gene for Oct-Binding Factor-1 (OBF1), a B-Cell-Specific Coactivator of Octamer-Binding Transcription Factors 1 and 2, to 11q23.1 by Somatic Cell Hybridization andin SituHybridization

1996 • 3 citations

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