(Q28360966)

1

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B Myllyluoma

2

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T Haltia

3

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M Taipale

4

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V Ollikainen

5

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T Ahonen

6

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A Voutilainen

7

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E Widén

Journal of Medical Genetics

9

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language of work or name

English

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publication date

October 2001

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published in

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volume

38

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issue

10

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page(s)

658-64

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cites work

A new gene (DYX3) for dyslexia is located on chromosome 2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Quantitative-trait locus for specific language and reading deficits on chromosome 6p

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Evidence for linkage of spelling disability to chromosome 15

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Functional disruption in the organization of the brain for reading in dyslexia

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Dopamine D3 receptor gene: organization, transcript variants, and polymorphism associated with schizophrenia

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Molecular cloning and functional expression of 5-HT1E-like rat and human 5-hydroxytryptamine receptor genes

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Quantitative trait locus for reading disability on chromosome 6

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Strategies for multilocus linkage analysis in humans

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Chromosomal localization of the human D3 dopamine receptor gene

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Parametric and nonparametric linkage analysis: a unified multipoint approach

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Two translocations of chromosome 15q associated with dyslexia

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

A physical map of 30,000 human genes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Rapid "automatized" naming (R.A.N): dyslexia differentiated from other learning disabilities

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Metabolic abnormalities in developmental dyslexia detected by 1H magnetic resonance spectroscopy.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Suggestive linkage of developmental dyslexia to chromosome 1p34-p36.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Evidence for a genetic aetiology in reading disability of twins.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Impaired visual word processing in dyslexia revealed with magnetoencephalography.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Normal activation of frontotemporal language cortex in dyslexia, as measured with oxygen 15 positron emission tomography

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Family patterns of developmental dyslexia: clinical findings.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734736

Specific dyslexia (congenital word-blindness); a clinical and genetic study

27 November 2018

1 reference

12 December 2020

Specific reading disability: identification of an inherited form through linkage analysis

1 reference

12 December 2020

Cosegregation of balanced translocation (1;2) with retarded speech development and dyslexia

1 reference

12 December 2020

Physiological, pathophysiological and therapeutic roles of 5-HT systems in learning and memory

1 reference

12 December 2020