(Q37519261)

20 August 2017

1 reference

title

Hearing impairment and pigmentary disturbance (English)

1 reference

20 August 2017

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Beighton P

1

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20 August 2017

Ramesar R

2

1 reference

20 August 2017

Winship I

3

1 reference

20 August 2017

Viljoen D

4

1 reference

20 August 2017

Greenberg J

5

1 reference

20 August 2017

Young K

6

1 reference

20 August 2017

Curtis D

7

1 reference

20 August 2017

Sellars S

8

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20 August 2017

language of work or name

English

0 references

publication date

1 January 1991

1 reference

Annals of the New York Academy of Sciences

20 August 2017

published in

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20 August 2017

volume

630

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20 August 2017

page(s)

152-166

1 reference

Childhood deafness in southern Africa. An aetiological survey of 3,064 deaf children.

20 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1991.TB19584.X

X-linked inheritance of ocular albinism with late-onset sensorineural deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1991.TB19584.X

Familial hemiplegic migraine, retinal degeneration, deafness, and nystagmus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1991.TB19584.X

Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1991.TB19584.X

Usher syndrome: definition and estimate of prevalence from two high-risk populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1991.TB19584.X

Localization of Usher syndrome type II to chromosome 1q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1991.TB19584.X

Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1991.TB19584.X

Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1991.TB19584.X

A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1991.TB19584.X

Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1991.TB19584.X

10.1111/J.1749-6632.1991.TB19584.X

21 January 2018

Identifiers

DOI

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20 August 2017

1 reference