(Q35625762)

9 August 2017

title

The genetics of deafness (English)

1 reference

9 August 2017

1 reference

Reardon W

1

1 reference

9 August 2017

Pembrey M

series ordinal

2

1 reference

9 August 2017

language of work or name

English

0 references

publication date

1 November 1990

1 reference

Archives of Disease in Childhood

9 August 2017

published in

1 reference

9 August 2017

volume

65

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9 August 2017

issue

11

1 reference

9 August 2017

page(s)

1196-1197

1 reference

Marshall/Stickler syndrome

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792620

X-linked mixed deafness with stapes fixation in a Mauritian kindred: linkage to Xq probe pDP34.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792620

The Stickler syndrome: evidence for close linkage to the structural gene for type II collagen

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792620

Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen 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=1792620

Identification of the cystic fibrosis gene: genetic analysis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792620

Localization of Usher syndrome type II to chromosome 1q.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792620

Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792620

Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792620

Genetic heterogeneity in osteogenesis imperfecta

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792620

Childhood deafness in the European community.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1792620

The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2248525

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A note on deaf mutism

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2248525

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/ADC.65.11.1196

1 reference

9 August 2017

1 reference

9 August 2017

1 reference