(Q33648769)

28 July 2017

title

Dominant cone dystrophy starting with blue cone involvement (English)

1 reference

28 July 2017

1 reference

van Schooneveld MJ

1

1 reference

28 July 2017

Went LN

series ordinal

2

1 reference

28 July 2017

Oosterhuis JA

series ordinal

3

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 June 1991

1 reference

28 July 2017

number of pages

5

1 reference

British Journal of Ophthalmology

inferred from page(s)

published in

1 reference

28 July 2017

volume

75

1 reference

28 July 2017

issue

6

1 reference

28 July 2017

page(s)

332-336

1 reference

The genetics of tritan disturbances.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1042376

Molecular genetics of inherited variation in human color vision

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1042376

Autosomal dominantly inherited macular dystrophy with preferential short-wavelength sensitive cone involvement.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1042376

Increment spectral sensitivity of hemizygotes and heterozygotes for different classes of colour vision

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1042376

Cone dystrophy, nyctalopia, and supernormal rod responses. A new retinal degeneration

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1042376

Color matching and foveal densitometry in patients and carriers of an X-linked progressive cone dystrophy

10 December 2018

1 reference

12 December 2020

New test for the detection of tritan defects evaluated in two surveys

1 reference

12 December 2020

Design of diagnostic tests for congenital and acquired colour vision defects

1 reference

12 December 2020

An electroretinographic and molecular genetic study of X-linked cone degeneration

1 reference

12 December 2020

Progressive cone dystrophy

1 reference

12 December 2020

Dominant Macular Degenerations the Cone Dystrophies

1 reference

12 December 2020

Cone Dystrophy with Dominant Inheritance

1 reference

12 December 2020

Identifiers

DOI

10.1136/BJO.75.6.332

1 reference

28 July 2017

1 reference

28 July 2017

1 reference