Otopathology in a case of type I Waardenburg's syndrome (Q42510181)

1 November 2017

title

Otopathology in a case of type I Waardenburg's syndrome (English)

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1 November 2017

S N Merchant

1

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M J McKenna

2

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1 November 2017

C T Baldwin

3

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A Milunsky

4

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J B Nadol

5

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publication date

1 September 2001

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Annals of Otology Rhinology and Laryngology

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number of pages

8

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based on heuristic

inferred from page(s)

published in

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volume

110

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1 November 2017

issue

9

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1 November 2017

page(s)

875-882

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An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

1 November 2017

cites work

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https://api.crossref.org/works/10.1177%2F000348940111000913

A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

Melanocyte System of the Endolymphatic Duct and Sac

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

Physiology and pathophysiology of inner ear melanin

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

Use of albino animals for auditory research

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

Strial dysfunction in mice with cochleo-saccular abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

Deafness as part of an hereditary syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

Inner ear anomalies in Waardenburg's syndrome associated with Hirschsprung's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

Temporal bone histopathologic findings of Waardenburg's syndrome: a case report.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

Distribution and features of melanocytes during inner ear development in pigmented and albino rats.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

Phenotypic variation in Waardenburg syndrome: mutational heterogeneity, modifier genes or polygenic background?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

Low-frequency hearing loss: perception of filtered speech, psychophysical tuning curves, and masking

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

Psychoacoustic tuning curves and averaged electroencephalic responses in a patient with low-frequency sensory-neural hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000348940111000913

10.1177/000348940111000913

21 January 2018

Identifiers

DOI

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1 November 2017

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