(Q35644079)

9 August 2017

title

A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p. (English)

1 reference

9 August 2017

1 reference

Anderson KL

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9 August 2017

Baird L

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9 August 2017

Lewis RA

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9 August 2017

Chinault AC

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9 August 2017

Otterud B

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9 August 2017

Leppert M

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9 August 2017

Lupski JR

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9 August 2017

language of work or name

English

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publication date

1 December 1995

1 reference

American Journal of Human Genetics

9 August 2017

published in

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9 August 2017

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9 August 2017

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9 August 2017

page(s)

1351-1363

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A type of degeneration involving the central zone of the choroid and retina.

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Dominant macular dystrophy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Characterization of the gene encoding human cone transducin alpha-subunit (GNAT2).

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

A first-generation physical map of the human genome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Histopathology and immunocytochemistry of the neurosensory retina in fundus flavimaculatus.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

The gene for the retinal pigment epithelium-specific protein RPE65 is localized to human 1p31 and mouse 3

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

The 1993-94 Généthon human genetic linkage map

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Stargardt's hereditary progressive macular degeneration

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Fluorescein studies in fundus flavimaculatus and drusen.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Dominant inheritance of Stargardt's disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Autosomal-dominant fundus flavimaculatus. Clinicopathologic correlation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Rapid identification of yeast artificial chromosome clones by matrix pooling and crude lysate PCR.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Mapping the whole human genome by fingerprinting yeast artificial chromosomes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Continuum of overlapping clones spanning the entire human chromosome 21q.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Isolation of chromosome 21-specific yeast artificial chromosomes from a total human genome library

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Evolution of the mammalian G protein alpha subunit multigene family

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Dinucleotide repeat polymorphism at the D1S167 locus

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Fundus Flavimaculatus and Stargardt's Disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Stargardt's Disease and Fundus Flavimaculatus

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Fundus fluorescein angiography in fundus flavimaculatus and Stargardts disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Stargardt's disease and fundus flavimaculatus

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Integrated human genome-wide maps constructed using the CEPH reference panel.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Isolation of single-copy human genes from a library of yeast artificial chromosome clones

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801408

Value of fluorescein angiography for fundus flavimaculatus

25 September 2018

1 reference

12 December 2020

Effect of vitamin A treatment on the prolongation of dark adaptation in Stargardt's dystrophy

1 reference

12 December 2020

Fundus flavimaculatus. Clinical, functional and histopathologic observations

1 reference

12 December 2020

Visual acuity loss in patients with Stargardt's macular dystrophy

1 reference

12 December 2020

Histopathology of Incipient Fundus Flavimaculatus

1 reference

12 December 2020

Dominantly inherited macular dystrophy with flecks (Stargardt)

1 reference

12 December 2020

Mapping of the human cone transducin alpha-subunit (GNAT2) gene to 1p13 and negative mutation analysis in patients with Stargardt disease.

1 reference

12 December 2020

A maculopathy associated with the 15257 mitochondrial DNA mutation

1 reference

12 December 2020

The dark choroid in systemic argyrosis

1 reference

12 December 2020

Fundus flavimaculatus of dominant heredity (apropos of 2 families). Nosological considerations on Stargardt's disease

1 reference

12 December 2020

Fundus flavimaculatus without maculopathy. A clinicopathologic study

1 reference

12 December 2020

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)

1 reference

12 December 2020

Long-term follow-up of dominant macular dystrophy with flecks (Stargardt)

1 reference

12 December 2020

Retinal function in Stargardt's disease and fundus flavimaculatus

1 reference

12 December 2020

Phenotypic Variation Including Retinitis Pigmentosa, Pattern Dystrophy, and Fundus Flavimaculatus in a Single Family With a Deletion of Codon 153 or 154 of the Peripherin/RDS Gene

1 reference

12 December 2020

[Fundus flavimaculatus]

1 reference

12 December 2020

Fundus flavimaculatus. A clinical classification

1 reference

12 December 2020

Identifiers

PMC publication ID

1801408

1 reference

9 August 2017

1 reference