(Q40697025)

22 September 2017

Clinical features and a follow-up study in a family with X-linked progressive cone-rod dystrophy (English)

1 reference

22 September 2017

Mäntyjärvi M

1

1 reference

22 September 2017

Nurmenniemi P

2

1 reference

22 September 2017

Partanen J

3

1 reference

22 September 2017

Myöhänen T

4

1 reference

22 September 2017

Peippo M

5

1 reference

22 September 2017

Alitalo T

6

1 reference

22 September 2017

language of work or name

1 reference

1 August 2001

1 reference

22 September 2017

1 reference

22 September 2017

79

1 reference

22 September 2017

4

1 reference

22 September 2017

359-365

1 reference

Progressive cone-rod degeneration

22 September 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

X linked progressive cone dystrophy with specific attention to carrier detection

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

X-linked progressive cone dystrophy. Clinical characteristics of affected males and female carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

21 January 2018

The cone degenerations

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

21 January 2018

X-linked cone dystrophy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

Clinical and electroretinographic findings of female carriers and affected males in a progressive X-linked cone-rod dystrophy (COD-1) pedigree

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

7 January 2021

CONE DYSFUNCTION SYNDROMES

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

7 January 2021

X-linked recessive cone dystrophy with tapetal-like sheen. A newly recognized entity with Mizuo-Nakamura phenomenon

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

7 January 2021

Progressive cone-rod dystrophy and high myopia in a Finnish family

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

7 January 2021

Standard for clinical electroretinography (1994 update)

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

7 January 2021

Cone Dystrophy with Dominant Inheritance

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

7 January 2021

X-linked cone dystrophy. An overlooked diagnosis?

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

7 January 2021

Progressive cone dystrophy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

7 January 2021

A new assessment of the normal ranges of the Farnsworth-Munsell 100-hue test scores

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2001.079004359.X

7 January 2021

10.1034/J.1600-0420.2001.079004359.X

Identifiers

DOI

1 reference

22 September 2017

1 reference