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Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25
scientific article
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instance of
scholarly article
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title
Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25
(English)
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author name string
D B Gould
series ordinal
1
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A J Mears
series ordinal
2
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W G Pearce
series ordinal
3
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M A Walter
series ordinal
4
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language of work or name
English
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publication date
September 1997
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published in
American Journal of Human Genetics
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volume
61
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page(s)
765-8
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issue
3
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cites work
Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715932
retrieved
7 April 2017
A second locus for Rieger syndrome maps to chromosome 13q14
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715932
retrieved
7 April 2017
Mutation of the PAX6 gene in patients with autosomal dominant keratitis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715932
retrieved
7 April 2017
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715932
retrieved
7 April 2017
Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715932
retrieved
7 April 2017
Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715932
retrieved
7 April 2017
Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715932
retrieved
7 April 2017
The human PAX6 gene is mutated in two patients with aniridia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715932
retrieved
7 April 2017
The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715932
retrieved
28 September 2017
Genetic heterogeneity in Rieger eye malformation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715932
retrieved
28 September 2017
Axenfeld-Rieger syndrome: a theory of mechanism and distinctions from the iridocorneal endothelial syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715932
retrieved
28 September 2017
Aniridia, congenital glaucoma, and hydrocephalus in a male infant with ring chromosome 6
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0002-9297%2807%2964340-7
retrieved
7 January 2021
Autosomal dominant iridogoniodysgenesis: genetic features
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9326342
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/S0002-9297(07)64340-7
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PMCID
1715932
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PubMed ID
9326342
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