Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients

Hannah Broadbent; Emily K. Farran; Esther Chin; Kay Metcalfe; May Tassabehji; Peter Turnpenny; Francis Sansbury; Emma Meaburn; Annette Karmiloff-Smith

doi:10.1186/1866-1955-6-18

Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients

Hannah Broadbent, Emily K. Farran, Esther Chin, Kay Metcalfe, May Tassabehji, Peter Turnpenny, Francis Sansbury, Emma Meaburn, Annette Karmiloff-Smith

Department of Psychology

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	1-13
Number of pages	13
Journal	Journal of Neurodevelopmental Disorders
Volume	6
Issue number	18
DOIs	https://doi.org/10.1186/1866-1955-6-18
Publication status	Published - 15 Jul 2014

Keywords

GTF2I
GTF2IRD1
LIMK1
Navigation
Visuospatial cognition
Williams syndrome

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10.1186/1866-1955-6-18Licence: CC BY

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title = "Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients",

keywords = "GTF2I, GTF2IRD1, LIMK1, Navigation, Visuospatial cognition, Williams syndrome",

author = "Hannah Broadbent and Farran, {Emily K.} and Esther Chin and Kay Metcalfe and May Tassabehji and Peter Turnpenny and Francis Sansbury and Emma Meaburn and Annette Karmiloff-Smith",

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doi = "10.1186/1866-1955-6-18",

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AU - Broadbent, Hannah

AU - Farran, Emily K.

AU - Chin, Esther

AU - Metcalfe, Kay

AU - Tassabehji, May

AU - Turnpenny, Peter

AU - Sansbury, Francis

AU - Meaburn, Emma

AU - Karmiloff-Smith, Annette

PY - 2014/7/15

Y1 - 2014/7/15

KW - GTF2I

KW - GTF2IRD1

KW - LIMK1

KW - Navigation

KW - Visuospatial cognition

KW - Williams syndrome

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U2 - 10.1186/1866-1955-6-18

DO - 10.1186/1866-1955-6-18

M3 - Article

AN - SCOPUS:84957966518

SN - 1866-1947

VL - 6

SP - 1

EP - 13

JO - Journal of Neurodevelopmental Disorders

JF - Journal of Neurodevelopmental Disorders

IS - 18

ER -

Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients

Keywords

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