(Q30577163)

25 June 2017

1 reference

title

Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome (English)

1 reference

25 June 2017

1 reference

Bellugi U

1

1 reference

25 June 2017

Lichtenberger L

2

1 reference

25 June 2017

Mills D

3

1 reference

25 June 2017

Galaburda A

4

1 reference

25 June 2017

Korenberg JR

5

1 reference

25 June 2017

1 May 1999

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25 June 2017

Trends in Neurosciences

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25 June 2017

22

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25 June 2017

197-207

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25 June 2017

5

1 reference

Memory Abilities in Children with Williams Syndrome

25 June 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Development itself is the key to understanding developmental disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Genetic approaches to cardiovascular disease. Supravalvular aortic stenosis, Williams syndrome, and long-QT syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

A survey of adults with Williams syndrome and idiopathic infantile hypercalcaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Linguistic abilities in Italian children with Williams syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Language and Williams syndrome: how intact is "intact"?

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Verbal and nonverbal abilities in the Williams syndrome phenotype: evidence for diverging developmental trajectories

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Word learning in a special population: do individuals with Williams syndrome obey lexical constraints?

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Syntax and morphology in Williams syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Adults with Williams syndrome. Preliminary study of social, emotional and behavioural difficulties.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Is there a social module? Language, face processing, and theory of mind in individuals with williams syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Narrative discourse in children with early focal brain injury

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Seeing either the forest or the trees: dissociation in visuospatial processing.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Unique profile of visuo-perceptual skills in a genetic syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Evidence from two genetic syndromes for a dissociation between verbal and visual-spatial short-term memory.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Specific neurobehavioral profile of Williams' syndrome is associated with neocerebellar hemispheric preservation.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Cerebral morphologic distinctions between Williams and Down syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Anomalous brain morphology on magnetic resonance images in Williams syndrome and Down syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

A specific deficit of dorsal stream function in Williams' syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Cytoarchitectonic anomalies in a genetically based disorder: Williams syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

The murine CYLN2 gene: genomic organization, chromosome localization, and comparison to the human gene that is located within the 7q11.23 Williams syndrome critical region

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

A novel human gene FKBP6 is deleted in Williams syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

A novel human gene, WSTF, is deleted in Williams syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Hemizygous deletion of the HPC-1/syntaxin 1A gene (STX1A) in patients with Williams syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

A 30 kb deletion within the elastin gene results in familial supravalvular aortic stenosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

Elastin point mutations cause an obstructive vascular disease, supravalvular aortic stenosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901397-1

7 January 2021

10.1016/S0166-2236(99)01397-1

Identifiers

DOI

1 reference

25 June 2017

1 reference