(Q40746166)

23 September 2017

A new locus for dominant drusen and macular degeneration maps to chromosome 6q14. (English)

1 reference

23 September 2017

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Kniazeva M

1

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23 September 2017

Traboulsi EI

2

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23 September 2017

Yu Z

3

1 reference

23 September 2017

Stefko ST

4

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23 September 2017

Gorin MB

5

1 reference

23 September 2017

Shugart YY

6

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23 September 2017

O'Connell JR

7

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23 September 2017

Blaschak CJ

8

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23 September 2017

Cutting G

9

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23 September 2017

Han M

10

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23 September 2017

Zhang K

11

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23 September 2017

language of work or name

English

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publication date

1 August 2000

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American Journal of Ophthalmology

23 September 2017

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23 September 2017

130

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23 September 2017

197-202

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23 September 2017

2

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The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16.

23 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

Malattia leventinese: refinement of the genetic locus and phenotypic variability in autosomal dominant macular drusen

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qter

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

North Carolina macular dystrophy is assigned to chromosome 6

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

Clinical spectrum of chromosome 6-linked autosomal dominant drusen and macular degeneration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

Comprehensive human genetic maps: individual and sex-specific variation in recombination

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

The human retinal degeneration slow (RDS) gene: Chromosome assignment and structure of the mRNA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

A dominant Stargardt's macular dystrophy locus maps to chromosome 13q34

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

A new locus for autosomal dominant stargardt-like disease maps to chromosome 4.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

An ancestral core haplotype defines the critical region harbouring the North Carolina macular dystrophy gene (MCDR1).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

A North Carolina macular dystrophy phenotype in a Belizean family maps to the MCDR1 locus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

A Gene Map of the Human Genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

Basic local alignment search tool

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

Molecular cloning and functional analysis of the adenovirus E1A-associated 300-kD protein (p300) reveals a protein with properties of a transcriptional adaptor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

Cloning of the gamma-aminobutyric acid (GABA) rho 1 cDNA: a GABA receptor subunit highly expressed in the retina

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

Identification of a putative gamma-aminobutyric acid (GABA) receptor subunit rho2 cDNA and colocalization of the genes encoding rho2 (GABRR2) and rho1 (GABRR1) to human chromosome 6q14-q21 and mouse chromosome 4

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

A novel truncated apolipoprotein B (apo B55) in a patient with familial hypobetalipoproteinemia and atypical retinitis pigmentosa

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900585-7

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0002-9394(00)00585-7

1 reference

23 September 2017

1 reference