(Q50447379)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19183916%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

[A new gene locus for an autosomal-dominant non-syndromic hearing impairment (DFNA 33) is situated on chromosome 13q34-qter] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19183916%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

Joerg Edgar Bohlender

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19183916%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Thomas Deufel

7

1 reference

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20 January 2020

author name string

D Bönsch

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19183916%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

C-M Schmidt

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19183916%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

P Scheer

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19183916%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

C Neumann

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19183916%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

A Am Zehnhoff-Dinnesen

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19183916%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

language of work or name

German

0 references

publication date

1 April 2009

1 reference

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20 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19183916%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

volume

57

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19183916%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

issue

4

1 reference

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20 January 2020

page(s)

371-376

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19183916%20AND%20SRC:MED&resulttype=core&format=json

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

20 January 2020

cites work

1 reference

12 December 2020

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

1 reference

12 December 2020

Parametric and nonparametric linkage analysis: a unified multipoint approach

1 reference

12 December 2020

Strategies for multilocus linkage analysis in humans

1 reference

12 December 2020

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans

1 reference

12 December 2020

PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype

1 reference

12 December 2020

Genetic epidemiology of hearing impairment

1 reference

12 December 2020

Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome

1 reference

12 December 2020

[A new locus for an autosomal dominant, non-syndromic hearing impairment (DFNA57) located on chromosome 19p13.2 and overlapping with DFNB15].

1 reference

12 December 2020

[Non-syndromic hereditary hearing impairment].

1 reference

12 December 2020

Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice

1 reference

12 December 2020

[Congenital hearing disorders in children. 1: Acquired hearing disorders]

1 reference

12 December 2020

Atp2b2, encoding plasma membrane Ca2+-ATPase type 2, (PMCA2) exhibits tissue-specific first exon usage in hair cells, neurons, and mammary glands of mice

1 reference

12 December 2020

The HUGO Gene Nomenclature Committee (HGNC).

1 reference

12 December 2020

Hearing molecules: contributions from genetic deafness

1 reference

12 December 2020

Non-syndromic, autosomal-recessive deafness

1 reference

12 December 2020

A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locus.

1 reference

12 December 2020

Hereditary sensorineural hearing loss: advances in molecular genetics and mutation analysis

1 reference

12 December 2020

Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.

1 reference

12 December 2020

10.1007/S00106-008-1832-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19183916%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference