(Q24675534)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940278%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940278%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

author name string

Mears AJ

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940278%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

Mirzayans F

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940278%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

Gould DB

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940278%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

Pearce WG

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940278%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

Walter MA

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940278%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

language of work or name

English

0 references

publication date

1 December 1996

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940278%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

21 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940278%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

volume

59

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940278%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

page(s)

1321-1327

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940278%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940278%20AND%20SRC:MED&resulttype=core&format=json

Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12)

21 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

Mutation of the PAX6 gene in patients with autosomal dominant keratitis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

A comprehensive genetic map of the human genome based on 5,264 microsatellites

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

Axenfeld-Rieger syndrome. A spectrum of developmental disorders

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

Genetic heterogeneity in Rieger eye malformation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

Terminal deletion of 6p: report of a new case.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

A case of partial monosomy 21q22.2 associated with Rieger's syndrome.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

Familial hypoplasia of the iris stroma associated with glaucoma

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

Partial deletion of chromosome 6p: delineation of the syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

Genetic linkage of familial open angle glaucoma to chromosome 1q21–q31

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914875

Autosomal dominant iridogoniodysgenesis: glaucoma management

28 November 2018

1 reference

12 December 2020

Autosomal dominant iridogoniodysgenesis: genetic features

1 reference

12 December 2020

Neural crest origin of trabecular meshwork cells and other structures of the anterior chamber

1 reference

12 December 2020

Distal deletion of the short arm of chromosome 6

1 reference

12 December 2020

A user-friendly Hypercard interface for human linkage analysis

1 reference

12 December 2020

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

1 reference

12 December 2020

Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region

1 reference

12 December 2020

Dominant goniodysgenesis with late congenital glaucoma. A re-examination of Berg's pedigree

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8940278%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference