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Cognitive characteristics of children with genetic syndromes
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Europe PubMed Central
PMCID
2435488
retrieved
16 August 2017
review article
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Europe PubMed Central
title
Cognitive characteristics of children with genetic syndromes
(English)
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Europe PubMed Central
PMCID
2435488
retrieved
16 August 2017
author name string
Tony J Simon
series ordinal
1
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Europe PubMed Central
PMCID
2435488
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16 August 2017
language of work or name
English
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publication date
1 July 2007
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PMCID
2435488
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16 August 2017
published in
Child and Adolescent Psychiatric Clinics of North America
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Europe PubMed Central
PMCID
2435488
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16 August 2017
volume
16
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Europe PubMed Central
PMCID
2435488
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16 August 2017
issue
3
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Europe PubMed Central
PMCID
2435488
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16 August 2017
page(s)
599-616
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Europe PubMed Central
PMCID
2435488
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16 August 2017
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A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome
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Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome.
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25 November 2018
Neural basis of genetically determined visuospatial construction deficit in Williams syndrome.
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Visual search in typically developing toddlers and toddlers with Fragile X or Williams syndrome.
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A cognitive characterization of dyscalculia in Turner syndrome.
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25 November 2018
Further delineation of the executive deficit in males with fragile-X syndrome.
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25 November 2018
The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory.
1 reference
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25 November 2018
Functional neuroanatomy of visuo-spatial working memory in Turner syndrome
1 reference
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PubMed Central
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25 November 2018
Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion.
1 reference
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25 November 2018
A neuropsychological profile of attention deficits in young males with fragile X syndrome.
1 reference
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PubMed Central
reference URL
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25 November 2018
Cognitive modularity and genetic disorders.
1 reference
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25 November 2018
Neural evidence linking visual object enumeration and attention.
1 reference
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25 November 2018
Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2435488
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25 November 2018
A process approach to describing mathematics difficulties in girls with Turner syndrome.
1 reference
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PubMed Central
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25 November 2018
Infants' metaphysics: the case of numerical identity.
1 reference
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PubMed Central
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25 November 2018
The psychoeducational characteristics of children with Turner syndrome.
1 reference
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PubMed Central
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25 November 2018
Brain anatomy in Turner syndrome: evidence for impaired social and spatial-numerical networks
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/17562581
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Specific arithmetic calculation deficits in children with Turner syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/17562581
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Williams syndrome cognitive profile also characterizes Velocardiofacial/DiGeorge syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/17562581
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Spatial and temporal processing in patients with Turner's syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/17562581
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/J.CHC.2007.03.002
1 reference
stated in
Europe PubMed Central
PMCID
2435488
retrieved
16 August 2017
PMCID
2435488
1 reference
stated in
Europe PubMed Central
PMCID
2435488
retrieved
16 August 2017
PubMed ID
17562581
1 reference
stated in
Europe PubMed Central
PMCID
2435488
retrieved
16 August 2017
ResearchGate publication ID
6273607
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