Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion). (Q48332601)

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scientific article published on 19 December 2006

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English	Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion).	scientific article published on 19 December 2006

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scholarly article

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Europe PubMed Central

PubMed publication ID

17180713

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10 February 2018

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Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion). (English)

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17180713

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10 February 2018

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main subject

autism

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autism spectrum disorder

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author

Wendy R Kates

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Wendy R Kates

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Kevin M Antshel

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1

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Alka Aneja

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2

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17180713

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Leslie Strunge

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3

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Jena Peebles

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4

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Wanda P Fremont

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5

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Kimberly Stallone

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6

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Nuria Abdulsabur

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7

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17180713

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Anne Marie Higgins

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8

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Robert J Shprintzen

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9

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17180713

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English

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publication date

19 December 2006

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17180713

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published in

Journal of Autism and Developmental Disorders

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17180713

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10 February 2018

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http://europepmc.org/abstract/MED/17180713

volume

37

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17180713

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10 February 2018

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http://europepmc.org/abstract/MED/17180713

issue

9

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Europe PubMed Central

PubMed publication ID

17180713

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10 February 2018

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http://europepmc.org/abstract/MED/17180713

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1776-1786

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cites work

Unusual brain growth patterns in early life in patients with autistic disorder: an MRI study.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS10803-006-0308-6

retrieved

21 January 2018

Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS10803-006-0308-6

retrieved

21 January 2018

Brain structural abnormalities in young children with autism spectrum disorder

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS10803-006-0308-6

retrieved

21 January 2018

Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability?

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS10803-006-0308-6

retrieved

21 January 2018

Comorbid psychiatric disorders in children with autism: interview development and rates of disorders

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Executive dysfunction and its relation to language ability in verbal school-age children with autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The amygdala and autism: implications from non‐human primate studies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuroanatomic variation in monozygotic twin pairs discordant for the narrow phenotype for autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Randomized trial of intensive early intervention for children with pervasive developmental disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile autism and affective disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism spectrum disorder in fragile X syndrome: communication, social interaction, and specific behaviors.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reliability and validity of MRI measurement of the amygdala and hippocampus in children with fragile X syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuroanatomical and neurocognitive differences in a pair of monozygous twins discordant for strictly defined autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Velocardiofacial syndrome: are structural changes in the temporal and mesial temporal regions related to schizophrenia?

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The functional neuroanatomy of social behaviour: changes in cerebral blood flow when people with autistic disorder process facial expressions

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gender-moderated dorsolateral prefrontal reductions in 22q11.2 Deletion Syndrome: implications for risk for schizophrenia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brief report: specific executive function profiles in three neurodevelopmental disorders

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Discriminative validity of a parent version of the Young Mania Rating Scale

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Convergent neuroanatomical and behavioural evidence of an amygdala hypothesis of autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Velo-cardio-facial syndrome: a distinctive behavioral phenotype

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of valproate in the treatment of mentally retarded persons with typical and atypical bipolar disorders.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic overshadowing reviewed and reconsidered

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Application of an automated parcellation method to the analysis of pediatric brain volumes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specific Genetic Disorders and Autism: Clinical Contribution Towards their Identification

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Executive dysfunction in autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brain mechanisms of emotion and emotional learning

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor structure of the Young Mania Rating Scale for use with youths ages 5 to 17 years

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Language skills in children with velocardiofacial syndrome (deletion 22q11.2).

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Social behavior profile in young males with fragile X syndrome: characteristics and specificity.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Toward a developmental neurobiology of autism.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Executive Function Deficits in High-Functioning Autistic Individuals: Relationship to Theory of Mind

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuropsychiatric disorders in the 22q11 deletion syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Down syndrome and comorbid autism-spectrum disorder: characterization using the aberrant behavior checklist.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intact and impaired memory functions in autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurological presentation of three patients with 22q11 deletion (CATCH 22 syndrome).

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Young children with Velo-Cardio-Facial syndrome (CATCH-22). Psychological and language phenotypes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychiatric disorders in individuals with pervasive developmental disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased prevalence of unprovoked seizures in patients with a 22q11.2 deletion

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The presentation of anxiety in children with pervasive developmental disorders

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Velo-cardio-facial syndrome.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amygdalar volume and behavioral development in autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): initial reliability and validity data

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Executive functions and developmental psychopathology

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The amygdala theory of autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 22q11 deletions are not found in autistic patients identified using strict diagnostic criteria. IMGSAC. International Molecular Genetics Study of Autism Consortium

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduced dorsal and orbital prefrontal gray matter volumes in schizophrenia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interhemispheric differences in the localization of psychological processes in man

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mania in Children With Pervasive Developmental Disorder Revisited

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Velo-cardio-facial syndrome and psychotic disorders: implications for psychiatric genetics

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuroanatomical substrates of social cognition dysfunction in autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Subgroups in autism: are there behavioural phenotypes typical of underlying medical conditions?

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Modified Checklist for Autism in Toddlers: an initial study investigating the early detection of autism and pervasive developmental disorders

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Outcomes of genetic evaluation in children with pervasive developmental disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brain anatomy and development in autism: review of structural MRI studies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autistic spectrum disorder and the fragile X premutation.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex differences in cognitive functioning in velocardiofacial syndrome (VCFS).

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation of the fusiform gyrus when individuals with autism spectrum disorder view faces

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism in tuberous sclerosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Superior temporal sulcus anatomical abnormalities in childhood autism: a voxel-based morphometry MRI study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neural correlates of facial affect processing in children and adolescents with autism spectrum disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Behavioral manifestations of autism in the first year of life

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Temperament in velocardiofacial syndrome.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Follow-up of children with autism spectrum disorders from age 2 to age 9.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal ventral temporal cortical activity during face discrimination among individuals with autism and Asperger syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Temporal lobe anatomy and psychiatric symptoms in velocardiofacial syndrome (22q11.2 deletion syndrome).

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychiatric disorders and behavioral problems in children with velocardiofacial syndrome: usefulness as phenotypic indicators of schizophrenia risk.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combining information from multiple sources in the diagnosis of autism spectrum disorders

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specifying PDD-NOS: a comparison of PDD-NOS, Asperger syndrome, and autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparing rates of psychiatric and behavior disorders in adolescents and young adults with severe intellectual disability with and without autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further evidence of intact working memory in autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of autism spectrum disorder.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17180713

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S10803-006-0308-6

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Europe PubMed Central

PubMed publication ID

17180713

retrieved

10 February 2018

reference URL

http://europepmc.org/abstract/MED/17180713

PubMed publication ID

17180713

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17180713

retrieved

10 February 2018

reference URL

http://europepmc.org/abstract/MED/17180713

ResearchGate publication ID

6618990

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