Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set. (Q31988981)

5 July 2017

title

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

1 reference

5 July 2017

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1 reference

L L Field

1

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5 July 2017

B J Kaplan

series ordinal

2

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5 July 2017

language of work or name

English

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publication date

1 November 1998

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American Journal of Human Genetics

5 July 2017

published in

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5 July 2017

volume

63

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5 July 2017

issue

5

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5 July 2017

page(s)

1448-1456

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

5 July 2017

cites work

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Affecteds-only linkage methods are not a panacea

21 June 2018

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Nonparametric simulation-based statistics for detecting linkage in general pedigrees

21 June 2018

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Susceptibility to insulin-dependent diabetes mellitus maps to a locus (IDDM11) on human chromosome 14q24.3-q31.

21 June 2018

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

21 June 2018

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Human glucagon-like peptide-1 receptor gene. Localization to chromosome band 6p21 by fluorescence in situ hybridization and linkage of a highly polymorphic simple tandem repeat DNA polymorphism to other markers on chromosome 6

21 June 2018

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Faster sequential genetic linkage computations

21 June 2018

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Two-locus models of disease: comparison of likelihood and nonparametric linkage methods

21 June 2018

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Quantitative trait locus for reading disability on chromosome 6

21 June 2018

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Mapping disease genes: family-based association studies

21 June 2018

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Reading disability in twins

21 June 2018

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Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

21 June 2018

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Evidence for a genetic aetiology in reading disability of twins

21 June 2018

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

21 June 2018

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The affected-pedigree-member method of linkage analysis

21 June 2018

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A simple salting out procedure for extracting DNA from human nucleated cells

21 June 2018

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Estimating the power of a proposed linkage study for a complex genetic trait.

21 June 2018

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Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

21 June 2018

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Specific deficits in component reading and language skills: genetic and environmental influences

21 June 2018

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Educational interventions in learning disabilities

21 June 2018

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Dinucleotide repeat polymorphism at the D6S89 locus

21 June 2018

1 reference

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Dinucleotide repeat polymorphism at the D6S105 locus

21 June 2018

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Neuroanatomic differences between dyslexic and normal readers on magnetic resonance imaging scans

21 June 2018

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Familial dyslexia: use of genetic linkage data to define subtypes

21 June 2018

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Tetranucleotide repeat polymorphism at the human coagulation factor XIII A subunit gene (F13A1).

21 June 2018

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DNA sequence polymorphism at the human tumor necrosis factor (TNF) locus. Numerous TNF/lymphotoxin alleles tagged by two closely linked microsatellites in the upstream region of the lymphotoxin (TNF-beta) gene

21 June 2018

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Reading disability, immune disorders and non-right-handedness: twin and family studies of their relations

21 June 2018

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The effects of parental immunoreactivity on pregnancy, birth, and cognitive development: maternal immune attack on the fetus?

21 June 2018

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The genetics of specific reading disability

21 June 2018

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Anomalous cerebral structure in dyslexia revealed with magnetic resonance imaging

21 June 2018

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Alzheimer's disease: a piscatorial trek.

31 October 2018

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Linkage detection by the Affected-Pedigree-Member method: what is really tested?

31 October 2018

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Brain morphology in developmental dyslexia and attention deficit disorder/hyperactivity

31 October 2018

1 reference

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Genetic models of reading disability

31 October 2018

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Adequacy of single-locus approximations for linkage analyses of oligogenic traits: extension to multigenerational pedigree structures

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12 December 2020

Identifiers

DOI

10.1086/302107

1 reference

release_4nfagskm2jbcznxajaemxoterm

5 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/4nfagskm2jbcznxajaemxoterm

24 November 2022

mapped directly with Wikidata item

PMC publication ID

1377556

1 reference

5 July 2017

1 reference