A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24 (Q24680575)

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3 November 2019

title

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

1 reference

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3 November 2019

1 reference

Verhoeven K

1

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3 November 2019

Van Camp G

2

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3 November 2019

Govaerts PJ

3

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3 November 2019

Balemans W

4

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3 November 2019

Schatteman I

5

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3 November 2019

Verstreken M

6

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3 November 2019

Van Laer L

7

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3 November 2019

Smith RJ

8

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3 November 2019

Brown MR

9

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3 November 2019

Van de Heyning PH

10

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3 November 2019

Somers T

11

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3 November 2019

Offeciers FE

12

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3 November 2019

Willems PJ

13

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3 November 2019

language of work or name

English

0 references

publication date

1 May 1997

1 reference

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American Journal of Human Genetics

3 November 2019

published in

1 reference

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volume

60

1 reference

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3 November 2019

issue

5

1 reference

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3 November 2019

page(s)

1168-1173

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Cloning, chromosomal localization and expression pattern of the POU domain gene Oct-11

3 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

Defective myosin VIIA gene responsible for Usher syndrome type 1B

7 April 2017

1 reference

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OBF-1, a novel B cell-specific coactivator that stimulates immunoglobulin promoter activity through association with octamer-binding proteins

7 April 2017

1 reference

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

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 and in situ hybridization

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

A B-cell coactivator of octamer-binding transcription factors

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

Report of the fourth international workshop on human chromosome 11 mapping 1994

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

Faster sequential genetic linkage computations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

Easy calculations of lod scores and genetic risks on small computers

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

Human/mouse homology relationships

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

Genetic epidemiology of hearing impairment

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

Localization of two genes for Usher syndrome type I to chromosome 11.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1712440

Optimization of microsatellite analysis for genetic mapping

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9150164

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9150164

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

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3 November 2019

PubMed publication ID

9150164

1 reference