North Carolina macular dystrophy: clinical features, genealogy, and genetic linkage analysis (Q34163723)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10360311%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

title

North Carolina macular dystrophy: clinical features, genealogy, and genetic linkage analysis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10360311%20AND%20SRC:MED&resulttype=core&format=json

North Carolina macular dystrophy

8 December 2019

main subject

1 reference

K W Small

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10360311%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

publication date

1 January 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10360311%20AND%20SRC:MED&resulttype=core&format=json

Transactions of the American Ophthalmological Society annual meeting

8 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10360311%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

volume

96

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10360311%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

page(s)

925-961

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10360311%20AND%20SRC:MED&resulttype=core&format=json

North Carolina macular dystrophy (MCDR1). A review and refined mapping to 6q14-q16.2.

8 December 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298417

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298417

A new dominant progressive foveal dystrophy.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298417

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298417

Computer-simulation methods in human linkage analysis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298417

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298417

North Carolina's dominant progressive foveal dystrophy: how progressive is it?

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298417

North Carolina macular dystrophy: exclusion map using RFLPs and microsatellites.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298417

North Carolina macular dystrophy and central areolar pigment epithelial dystrophy. One family, one disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298417

Strategies for multilocus linkage analysis in humans

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298417

Central areolar pigment epithelial dystrophy

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298417

An inherited central retinal pigment epithelial dystrophy

28 October 2018

1 reference

12 December 2020

Autosomal dominant central pigment epithelial and choroidal degeneration

1 reference

12 December 2020

Central areolar pigment epithelial dystrophy

1 reference

12 December 2020

North Carolina macular dystrophy, revisited

1 reference

12 December 2020

North Carolina macular dystrophy is assigned to chromosome 6

1 reference

12 December 2020

Clinical and genetic evidence for autosomal dominant North Carolina macular dystrophy in a German family

1 reference

12 December 2020

Hereditary Macular Degeneration and Amino-Aciduria

1 reference

12 December 2020

Foveal cone electroretinograms in retinitis pigmentosa and juvenile maular degeneration

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10360311%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

PubMed publication ID

10360311

1 reference