(Q35643624)

9 August 2017

The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian population (English)

1 reference

9 August 2017

1 reference

M A Maw

1

1 reference

9 August 2017

D R Allen-Powell

2

1 reference

9 August 2017

R J Goodey

3

1 reference

9 August 2017

I A Stewart

4

1 reference

9 August 2017

D J Nancarrow

5

1 reference

9 August 2017

N K Hayward

6

1 reference

9 August 2017

R J Gardner

7

1 reference

9 August 2017

language of work or name

English

0 references

publication date

1 September 1995

1 reference

American Journal of Human Genetics

9 August 2017

1 reference

9 August 2017

57

1 reference

9 August 2017

3

1 reference

9 August 2017

629-635

1 reference

The mutational load due to detrimental genes in man

9 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801273

A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801273

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801273

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801273

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801273

The genetics of sensorineural deafness

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801273

Estimated number of loci for autosomal recessive severe nerve deafness within the Israeli Jewish population, with implications for genetic counseling

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801273

Symposium on sensorineural hearing loss in children: early detection and intervention. Genetic factors in deafness of early life

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801273

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801273

Hereditary deaf mutism, with particular reference to Northern Ireland

7 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7668291

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMCID

1801273

1 reference

9 August 2017

1 reference