(Q34388570)

1 August 2017

title

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

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1 August 2017

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quantitative trait locus

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1

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1 August 2017

9

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1 August 2017

J Lamb

3

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author name string

A J Marlow

2

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1 August 2017

E Maestrini

4

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1 August 2017

D F Williams

5

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1 August 2017

A J Richardson

6

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1 August 2017

D E Weeks

7

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1 August 2017

J F Stein

8

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1 August 2017

language of work or name

English

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publication date

1 January 1999

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American Journal of Human Genetics

1 August 2017

published in

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1 August 2017

volume

64

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1 August 2017

issue

1

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1 August 2017

page(s)

146-156

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

1 August 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: summary of GAW10 contributions

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

Heterogeneity in rates of recombination in the 6-Mb region telomeric to the human major histocompatibility complex

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

Using genetics to dissect cognition

6 July 2018

1 reference

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A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

6 July 2018

1 reference

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Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

6 July 2018

1 reference

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

6 July 2018

1 reference

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Varieties of developmental dyslexia.

6 July 2018

1 reference

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Robust variance-components approach for assessing genetic linkage in pedigrees

6 July 2018

1 reference

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

Quantitative trait locus for reading disability on chromosome 6

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

Complete multipoint sib-pair analysis of qualitative and quantitative traits

6 July 2018

1 reference

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Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

6 July 2018

1 reference

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Multiple regression analysis of twin data

6 July 2018

1 reference

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Evidence for a genetic aetiology in reading disability of twins.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

Dyslexia and chromosome 15 heteromorphism: negative lod score in a Danish material.

6 July 2018

1 reference

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Left-handedness and immune disorders in familial dyslexics

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

The affected-pedigree-member method of linkage analysis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

Prevalence of reading disability in boys and girls. Results of the Connecticut Longitudinal Study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

Immune and autoimmune diseases in dyslexic children

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

Evidence for major gene transmission of developmental dyslexia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

The concept of specific reading retardation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

Statistical validity of the Haseman-Elston sib-pair test in small samples.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

Recombination rates across the HLA complex: use of microsatellites as a rapid screen for recombinant chromosomes.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

The assessment of children with specific reading difficulties (dyslexia) using the British Ability Scales.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377712

The investigation of linkage between a quantitative trait and a marker locus

27 October 2018

1 reference

12 December 2020

The information contained in multiple sibling pairs

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic models of reading disability

1 reference

12 December 2020

Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mapping

1 reference

12 December 2020

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

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12 December 2020

Detection of major genes underlying several quantitative traits associated with a common disease using different ascertainment schemes

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12 December 2020

Identifiers

DOI

10.1086/302190

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1 August 2017

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1 August 2017

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