Allelic variants of DYX1C1 are not associated with dyslexia in India. - Test2 - elhamkhani - TriplyDB

Allelic variants of DYX1C1 are not associated with dyslexia in India.

Allelic variants of DYX1C1 are not associated with dyslexia in India.

http://www.wikidata.org/entity/Q33735905

about

An informatics approach to integrating genetic and neurological data in speech and language neuroscience.Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.An examination of candidate gene SNPs for dyslexia in an Indian sample.ATP2C2 and DYX1C1 are putative modulators of dyslexia-related MMR.Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: an integrated meta-analysis.

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P2860

Allelic variants of DYX1C1 are not associated with dyslexia in India.

http://www.wikidata.org/entity/Q33735905

description

2008 nî lūn-bûn

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2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2008 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

Allelic variants of DYX1C1 are not associated with dyslexia in India.

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Allelic variants of DYX1C1 are not associated with dyslexia in India.

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Allelic variants of DYX1C1 are not associated with dyslexia in India.

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Allelic variants of DYX1C1 are not associated with dyslexia in India.

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Allelic variants of DYX1C1 are not associated with dyslexia in India.

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Allelic variants of DYX1C1 are not associated with dyslexia in India.

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Indian Journal of Human Genetics

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Allelic variants of DYX1C1 are not associated with dyslexia in India.

@en

P2093

Nallur Basappa Ramachandra

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Pushpa Saviour

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Rajasekhara Reddy Ravuri

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Satish Kumar

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U Kiran

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V R Rao

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P2860

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia

A transcription map of the 6p22.3 reading disability locus identifying candidate genes

DCDC2 is associated with reading disability and modulates neuronal development in the brain.

Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation

Evidence for linkage of spelling disability to chromosome 15

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK

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

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

Quantitative trait locus for reading disability on chromosome 6

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