(Q50503069)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9849679%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

title

Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome (English)

1 reference

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7 December 2019

1 reference

8

1 reference

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7 December 2019

author name string

C W Cremers

1

1 reference

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7 December 2019

R J Admiraal

2

1 reference

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7 December 2019

P L Huygen

3

1 reference

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7 December 2019

C Bolder

4

1 reference

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7 December 2019

L A Everett

5

1 reference

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7 December 2019

F B Joosten

6

1 reference

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7 December 2019

E D Green

7

1 reference

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7 December 2019

B J Otten

9

1 reference

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7 December 2019

publication date

1 October 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9849679%20AND%20SRC:MED&resulttype=core&format=json

International Journal of Pediatric Otorhinolaryngology

7 December 2019

published in

1 reference

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7 December 2019

volume

45

1 reference

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7 December 2019

issue

2

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7 December 2019

page(s)

113-123

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Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndrome

7 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2898%2900123-2

7 January 2021

ASSOCIATION OF CONGENITAL DEAFNESS WITH GOITRE (PENDRED'S SYNDROME) A STUDY OF 207 FAMILIES.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2898%2900123-2

7 January 2021

An approach to the causes of early childhood deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2898%2900123-2

7 January 2021

Two frequent missense mutations in Pendred syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2898%2900123-2

7 January 2021

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2898%2900123-2

7 January 2021

Radiological malformations of the ear in Pendred syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2898%2900123-2

7 January 2021

Pendred's syndrome. Acoustic, vestibular and radiological findings in 17 unrelated patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2898%2900123-2

7 January 2021

Pendred's syndrome with episodic vertigo, tinnitus and vomiting and normal bithermal caloric responses.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2898%2900123-2

7 January 2021

Phenotypic manifestations of branchio-oto-renal syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2898%2900123-2

7 January 2021

A mutation in PDS causes non-syndromic recessive deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2898%2900123-2

7 January 2021

The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7q

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2898%2900123-2

7 January 2021

10.1016/S0165-5876(98)00123-2

Identifiers

DOI

1 reference

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7 December 2019

1 reference