(Q34125294)

31 July 2017

DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34. (English)

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sensorineural hearing loss

31 July 2017

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1 reference

10

Mark Lathrop

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31 July 2017

Christine Petit

11

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Dominique Weil

9

object named as

Dominique Weil

1 reference

31 July 2017

3

Sébastien Chardenoux

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31 July 2017

8

Jacques Loiselet

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31 July 2017

Mirna Mustapha

1

1 reference

31 July 2017

Eliane Chouery

2

1 reference

31 July 2017

Mohamed Naboulsi

4

1 reference

31 July 2017

Joël Paronnaud

5

1 reference

31 July 2017

Arnaud Lemainque

6

1 reference

31 July 2017

André Mégarbané

7

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31 July 2017

1 March 2002

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European Journal of Human Genetics

31 July 2017

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31 July 2017

10

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31 July 2017

210-212

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31 July 2017

3

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200780

31 July 2017

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cites work

Molecular genetics of hearing loss

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

Usher syndrome: from genetics to pathogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

Inherited hearing defects in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

Auditory and vestibular mouse mutants: models for human deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

Linkage analysis of the whirler deafness gene on mouse chromosome 4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

Genetic mapping of the whirler mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

A Gene Responsible for a Sensorineural Nonsyndromic Recessive Deafness Maps to Chromosome 2p22-23

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

Genotyping Procedures in Linkage Mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200780

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EJHG.5200780

1 reference

31 July 2017

1 reference