Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays (Q83320994)

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21 January 2020

title

Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays (English)

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21 January 2020

7

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21 January 2020

author name string

L Dai

1

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21 January 2020

U Bellugi

2

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21 January 2020

X-N Chen

3

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21 January 2020

A M Pulst-Korenberg

4

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21 January 2020

A Järvinen-Pasley

5

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21 January 2020

T Tirosh-Wagner

6

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21 January 2020

J Graham

8

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21 January 2020

D Mills

9

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21 January 2020

Y Searcy

10

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21 January 2020

J R Korenberg

11

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21 January 2020

publication date

1 March 2009

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American Journal of Medical Genetics

21 January 2020

published in

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21 January 2020

volume

149A

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21 January 2020

issue

3

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21 January 2020

page(s)

302-314

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Partial deletion of the critical 1.5 Mb interval in Williams-Beuren syndrome

21 January 2020

cites work

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12 December 2020

Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23

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12 December 2020

GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region.

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12 December 2020

"Everybody in the world is my friend" hypersociability in young children with Williams syndrome

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12 December 2020

Self concept in people with Williams syndrome and Prader–Willi syndrome

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12 December 2020

An experiment of nature: brain anatomy parallels cognition and behavior in Williams syndrome

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12 December 2020

Central and peripheral effects of oxytocin administration in prairie voles (Microtus ochrogaster).

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12 December 2020

A cognitive and behavioural phenotype in williams syndrome

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12 December 2020

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

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12 December 2020

Increased Fos expression in oxytocin neurons following masculine sexual behavior

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12 December 2020

Social-emotional and behavioral adjustment in children with Williams-Beuren syndrome.

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12 December 2020

Human cDNA mapping using a high-resolution R-banding technique and fluorescence in situ hybridization

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12 December 2020

Second-order belief attribution in Williams syndrome: intact or impaired?

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12 December 2020

Conversion of diploidy to haploidy

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12 December 2020

A componential view of theory of mind: evidence from Williams syndrome

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12 December 2020

Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes

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12 December 2020

Williams syndrome: cognition, personality, and adaptive behavior

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12 December 2020

I. The neurocognitive profile of Williams Syndrome: a complex pattern of strengths and weaknesses

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12 December 2020

II. Hypersociability in Williams Syndrome.

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12 December 2020

VI. Genome structure and cognitive map of Williams syndrome

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12 December 2020

Biochemistry and biology of the inducible multifunctional transcription factor TFII-I.

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12 December 2020

Prevalence estimation of Williams syndrome

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12 December 2020

Using case study comparisons to explore genotype-phenotype correlations in Williams-Beuren syndrome

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12 December 2020

Distinctive Personality Characteristics of 8-, 9-, and 10-Year-Olds With Williams Syndrome

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12 December 2020

Mutational mechanisms of Williams-Beuren syndrome deletions

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12 December 2020

Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletion.

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12 December 2020

Behavioral and emotional disturbance in individuals with Williams syndrome

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12 December 2020

Personality characteristics and behaviour problems in individuals of different ages with Williams syndrome

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12 December 2020

Plasma oxytocin levels in autistic children.

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12 December 2020

Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes

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12 December 2020

Refining behavioral phenotypes: personality-motivation in Williams and Prader-Willi syndromes

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12 December 2020

Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorder

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12 December 2020

Neural correlates of genetically abnormal social cognition in Williams syndrome

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12 December 2020

Music and anxiety in Williams syndrome: a harmonious or discordant relationship?

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12 December 2020

Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.

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12 December 2020

GTF2IRD1 in craniofacial development of humans and mice

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12 December 2020

Is everybody always my friend? Perception of approachability in Williams syndrome

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12 December 2020

Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletions

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12 December 2020

High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays

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12 December 2020

Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour

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12 December 2020

Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes

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12 December 2020

Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development

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12 December 2020

An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism

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12 December 2020

Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome

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12 December 2020

The neuropsychological basis of hypersociability in Williams and Down syndrome

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12 December 2020

Nature and nurture: Williams syndrome across cultures

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12 December 2020

Diminished plasma oxytocin in schizophrenic patients with neuroendocrine dysfunction and emotional deficits

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12 December 2020

Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior

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12 December 2020

Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted mice

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12 December 2020

Expression of BEN, a member of TFII-I family of transcription factors, during mouse pre- and postimplantation development

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12 December 2020

Identifiers

DOI

10.1002/AJMG.A.32652

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21 January 2020

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21 January 2020

PubMed publication ID

19205026

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