Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.

Zobrazit další vydání (1)

AIM: Sex chromosome aneuploidies increase the risk of spoken or written language disorders but individuals with specific language impairment (SLI) or dyslexia do not routinely undergo cytogenetic analysis. We assess the frequency of sex chromosome aneuploidies in individuals with language impairment...

Podrobná bibliografie
Hlavní autoři:	Simpson, N, Addis, L, Brandler, WM, Slonims, V, Clark, A, Watson, J, Scerri, T, Hennessy, E, Bolton, P, Conti-Ramsden, G, Fairfax, B, Knight, J, Stein, J, Talcott, J, O'Hare, A, Baird, G, Paracchini, S, Fisher, SE, Newbury, D
Médium:	Journal article
Jazyk:	English
Vydáno:	Blackwell Publishing Ltd 2014

Podobné jednotky

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
Autor: Simpson, N, a další
Vydáno: (2014)

PCSK6 is associated with handedness in individuals with dyslexia
Autor: Richardson, A, a další
Vydáno: (2011)

PCSK6 is associated with handedness in individuals with dyslexia.
Autor: Scerri, T, a další
Vydáno: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
Autor: Newbury, D, a další
Vydáno: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
Autor: Newbury, D, a další
Vydáno: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
Autor: Newbury, D, a další
Vydáno: (2011)

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language- Impaired Subjects
Autor: Richardson, A, a další
Vydáno: (2011)

The genetic lexicon of dyslexia.
Autor: Paracchini, S, a další
Vydáno: (2007)

Correction: identification of candidate genes for dyslexia susceptibility on chromosome 18.
Autor: Scerri, T, a další
Vydáno: (2010)

Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
Autor: Simpson, N, a další
Vydáno: (2015)

Identification of candidate genes for dyslexia susceptibility on chromosome 18
Autor: Richardson, A, a další
Vydáno: (2010)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
Autor: Scerri, T, a další
Vydáno: (2010)

Associations of HLA alleles with specific language impairment.
Autor: Nudel, R, a další
Vydáno: (2014)

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
Autor: Nudel, R, a další
Vydáno: (2014)

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
Autor: Nudel, R, a další
Vydáno: (2014)

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
Autor: Scerri, T, a další
Vydáno: (2012)

The DCDC2 deletion is not a risk factor for dyslexia
Autor: Scerri, T, a další
Vydáno: (2017)

The genetics of handedness and dyslexia
Autor: Brandler, W
Vydáno: (2014)

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.
Autor: Paracchini, S, a další
Vydáno: (2008)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
Autor: Thomas S Scerri, a další
Vydáno: (2010-10-01)

Cerebellar morphology in developmental dyslexia.
Autor: Rae, C, a další
Vydáno: (2002)

Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18.
Autor: Thomas S. Scerri, a další
Vydáno: (2010-01-01)

Genome-wide screening for DNA variants associated with reading and language traits.
Autor: Gialluisi, A, a další
Vydáno: (2014)

Further evidence that KIAA0319 is associated with developmental dyslexia
Autor: Harold, D, a další
Vydáno: (2006)

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
Autor: Dennis, M, a další
Vydáno: (2009)

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK.
Autor: Scerri, T, a další
Vydáno: (2004)

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.
Autor: Thomas S Scerri, a další
Vydáno: (2012-01-01)

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill
Autor: Brandler, WM, a další
Vydáno: (2013)

Lack of asymmetry characterises the cerebellum in developmental dyslexia
Autor: Harasty, J, a další
Vydáno: (2001)

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
Autor: Harold, D, a další
Vydáno: (2006)

The perception of "sine-wave speech" by adults with developmental dyslexia.
Autor: Rosner, B, a další
Vydáno: (2003)

Multivariate multipoint linkage analysis of QTL in dyslexia
Autor: Marlow, A, a další
Vydáno: (2002)

Dyslexia Genetics
Autor: Stein, J
Vydáno: (2008)

CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
Autor: Newbury, D, a další
Vydáno: (2009)

Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia
Autor: Harold, D, a další
Vydáno: (2006)

The cerebellum and dyslexia.
Autor: Stoodley, C, a další
Vydáno: (2011)

What is Developmental Dyslexia?
Autor: Stein, J
Vydáno: (2018)

Does dyslexia exist?
Autor: Stein, J
Vydáno: (2017)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
Autor: Paracchini, S, a další
Vydáno: (2006)

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
Autor: Megan Y Dennis, a další
Vydáno: (2009-03-01)