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

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

Visa andra versioner (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...

Full beskrivning

Bibliografiska uppgifter
Huvudupphovsmän:	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
Materialtyp:	Journal article
Språk:	English
Publicerad:	Blackwell Publishing Ltd 2014

Liknande verk

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
av: Simpson, N, et al.
Publicerad: (2014)

PCSK6 is associated with handedness in individuals with dyslexia
av: Richardson, A, et al.
Publicerad: (2011)

PCSK6 is associated with handedness in individuals with dyslexia.
av: Scerri, T, et al.
Publicerad: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
av: Newbury, D, et al.
Publicerad: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
av: Newbury, D, et al.
Publicerad: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
av: Newbury, D, et al.
Publicerad: (2011)

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language- Impaired Subjects
av: Richardson, A, et al.
Publicerad: (2011)

The genetic lexicon of dyslexia.
av: Paracchini, S, et al.
Publicerad: (2007)

Correction: identification of candidate genes for dyslexia susceptibility on chromosome 18.
av: Scerri, T, et al.
Publicerad: (2010)

Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
av: Simpson, N, et al.
Publicerad: (2015)

Identification of candidate genes for dyslexia susceptibility on chromosome 18
av: Richardson, A, et al.
Publicerad: (2010)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
av: Scerri, T, et al.
Publicerad: (2010)

Associations of HLA alleles with specific language impairment.
av: Nudel, R, et al.
Publicerad: (2014)

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
av: Nudel, R, et al.
Publicerad: (2014)

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
av: Nudel, R, et al.
Publicerad: (2014)

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
av: Scerri, T, et al.
Publicerad: (2012)

The DCDC2 deletion is not a risk factor for dyslexia
av: Scerri, T, et al.
Publicerad: (2017)

The genetics of handedness and dyslexia
av: Brandler, W
Publicerad: (2014)

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.
av: Paracchini, S, et al.
Publicerad: (2008)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
av: Thomas S Scerri, et al.
Publicerad: (2010-10-01)

Cerebellar morphology in developmental dyslexia.
av: Rae, C, et al.
Publicerad: (2002)

Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18.
av: Thomas S. Scerri, et al.
Publicerad: (2010-01-01)

Genome-wide screening for DNA variants associated with reading and language traits.
av: Gialluisi, A, et al.
Publicerad: (2014)

Further evidence that KIAA0319 is associated with developmental dyslexia
av: Harold, D, et al.
Publicerad: (2006)

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
av: Dennis, M, et al.
Publicerad: (2009)

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

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.
av: Thomas S Scerri, et al.
Publicerad: (2012-01-01)

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill
av: Brandler, WM, et al.
Publicerad: (2013)

Lack of asymmetry characterises the cerebellum in developmental dyslexia
av: Harasty, J, et al.
Publicerad: (2001)

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
av: Harold, D, et al.
Publicerad: (2006)

The perception of "sine-wave speech" by adults with developmental dyslexia.
av: Rosner, B, et al.
Publicerad: (2003)

Multivariate multipoint linkage analysis of QTL in dyslexia
av: Marlow, A, et al.
Publicerad: (2002)

Dyslexia Genetics
av: Stein, J
Publicerad: (2008)

CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
av: Newbury, D, et al.
Publicerad: (2009)

Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia
av: Harold, D, et al.
Publicerad: (2006)

The cerebellum and dyslexia.
av: Stoodley, C, et al.
Publicerad: (2011)

What is Developmental Dyslexia?
av: Stein, J
Publicerad: (2018)

Does dyslexia exist?
av: Stein, J
Publicerad: (2017)

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

A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
av: Megan Y Dennis, et al.
Publicerad: (2009-03-01)