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A new gene (DYX3) for dyslexia is located on chromosome 2
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
title
A new gene (DYX3) for dyslexia is located on chromosome 2
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
main subject
dyslexia
0 references
author name string
Fagerheim T
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
Raeymaekers P
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
Tønnessen FE
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
Pedersen M
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
Tranebjaerg L
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
Lubs HA
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
language of work or name
English
0 references
publication date
1 September 1999
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
volume
36
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
issue
9
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
page(s)
664-669
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
cites work
Quantitative-trait locus for specific language and reading deficits on chromosome 6p
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=1734428
retrieved
7 April 2017
Evidence for linkage of spelling disability to chromosome 15
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=1734428
retrieved
7 April 2017
Functional disruption in the organization of the brain for reading in dyslexia
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=1734428
retrieved
7 April 2017
Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
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=1734428
retrieved
7 April 2017
Calcineurin A alpha (PPP3CA), calcineurin A beta (PPP3CB) and calcineurin B (PPP3R1) are located on human chromosomes 4, 10q21-->q22 and 2p16-->p15 respectively
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=1734428
retrieved
7 April 2017
Physiological and anatomical evidence for a magnocellular defect in developmental dyslexia
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=1734428
retrieved
7 April 2017
A comprehensive genetic map of the human genome based on 5,264 microsatellites
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=1734428
retrieved
7 April 2017
Strategies for multilocus linkage analysis in humans
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=1734428
retrieved
7 April 2017
Quantitative trait locus for reading disability on chromosome 6
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=1734428
retrieved
7 April 2017
Parametric and nonparametric linkage analysis: a unified multipoint approach
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=1734428
retrieved
7 April 2017
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
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=1734428
retrieved
7 April 2017
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia
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=1734428
retrieved
28 September 2017
Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set.
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=1734428
retrieved
28 September 2017
Neurobiological basis of speech: a case for the preeminence of temporal processing
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=1734428
retrieved
28 September 2017
Linkage strategies for genetically complex traits. I. Multilocus models
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=1734428
retrieved
28 September 2017
Evidence for major gene transmission of developmental dyslexia
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=1734428
retrieved
28 September 2017
Using genetics to dissect cognition
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=1734428
retrieved
30 May 2018
Suggestive linkage of developmental dyslexia to chromosome 1p34-p36.
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=1734428
retrieved
30 May 2018
Dyslexia and chromosome 15 heteromorphism: negative lod score in a Danish material.
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=1734428
retrieved
30 May 2018
Specific deficits in component reading and language skills: genetic and environmental influences.
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=1734428
retrieved
30 May 2018
Impaired visual word processing in dyslexia revealed with magnetoencephalography.
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=1734428
retrieved
28 November 2018
Specific reading disability: identification of an inherited form through linkage analysis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10507721
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Cosegregation of balanced translocation (1;2) with retarded speech development and dyslexia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10507721
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Contrast sensitivity in dyslexia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10507721
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
1734428
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
PubMed publication ID
10507721
1 reference
stated in
Europe PubMed Central
PMC publication ID
1734428
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10507721%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
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