(Q35559715)

8 August 2017

title

Two translocations of chromosome 15q associated with dyslexia (English)

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8 August 2017

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8 August 2017

J Nopola-Hemmi

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8 August 2017

M Taipale

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8 August 2017

T Haltia

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8 August 2017

A E Lehesjoki

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8 August 2017

A Voutilainen

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8 August 2017

language of work or name

English

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publication date

1 October 2000

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Journal of Medical Genetics

8 August 2017

published in

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8 August 2017

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8 August 2017

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8 August 2017

page(s)

771-775

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

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757170

Comprehensive human genetic maps: individual and sex-specific variation in recombination

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757170

Evidence for linkage of spelling disability to chromosome 15

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757170

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757170

The genetics of cornea plana congenita

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757170

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757170

Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757170

Quantitative trait locus for reading disability on chromosome 6

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757170

A YAC contig map of the human genome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757170

Evidence for a genetic aetiology in reading disability of twins.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757170

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1757170

Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11015455

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11015455

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11015455

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.37.10.771

1 reference

8 August 2017

1 reference

8 August 2017

1 reference