(Q36983039)

17 August 2017

Histopathology of nonsyndromic autosomal dominant midfrequency sensorineural hearing loss (English)

1 reference

17 August 2017

1 reference

Fayez Bahmad

1

1 reference

17 August 2017

Jennifer O'Malley

series ordinal

2

1 reference

17 August 2017

Lisbeth Tranebjaerg

series ordinal

3

1 reference

17 August 2017

Saumil N Merchant

series ordinal

4

1 reference

17 August 2017

1 August 2008

1 reference

17 August 2017

Otology & Neurotology

1 reference

17 August 2017

29

1 reference

17 August 2017

5

1 reference

17 August 2017

601-606

1 reference

Polyester wax: a new embedding medium for the histopathologic study of human temporal bones

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

V Dominant Midfrequency Hearing Loss

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

Hereditary nerve deafness. A follow-up of four cases in one family.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

Dominant hereditary nerve deafness.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

Autosomal dominant midfrequency hearing impairment.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13).

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21).

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

The phenotype of DFNA13/COL11A2: nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587055

Familial Progressive Sensorineural Deafness

4 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18665028

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1097/MAO.0B013E3181778245

1 reference

17 August 2017

1 reference

17 August 2017

PubMed publication ID

18665028

1 reference