Literature DB >> 10521286

Visuospatial construction.

C B Mervis1, B F Robinson, J R Pani.   

Abstract

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Year:  1999        PMID： 10521286      PMCID： PMC1288273          DOI： 10.1086/302633

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  12 in total

1.  The separability of working memory resources for spatial thinking and language processing: an individual differences approach.

Authors:  P Shah; A Miyake
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2.  Mental rotation of three-dimensional objects.

Authors:  R N Shepard; J Metzler
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4.  Is the gender difference in mental rotation disappearing?

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5.  Spatial reference systems in the comprehension of rotational motion.

Authors:  J R Pani; D Dupree
Journal:  Perception       Date:  1994       Impact factor: 1.490

Review 6.  Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome.

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

Authors:  A K Ewart; C A Morris; D Atkinson; W Jin; K Sternes; P Spallone; A D Stock; M Leppert; M T Keating
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8.  Supravalvular aortic stenosis cosegregates with a familial 6; 7 translocation which disrupts the elastin gene.

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9.  LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition.

Authors:  J M Frangiskakis; A K Ewart; C A Morris; C B Mervis; J Bertrand; B F Robinson; B P Klein; G J Ensing; L A Everett; E D Green; C Pröschel; N J Gutowski; M Noble; D L Atkinson; S J Odelberg; M T Keating
Journal:  Cell       Date:  1996-07-12       Impact factor: 41.582

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

Authors:  M Tassabehji; K Metcalfe; A Karmiloff-Smith; M J Carette; J Grant; N Dennis; W Reardon; M Splitt; A P Read; D Donnai
Journal:  Am J Hum Genet       Date:  1999-01       Impact factor: 11.025
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2.  Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.

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Review 3.  Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.

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8.  A genetic model for understanding higher order visual processing: functional interactions of the ventral visual stream in Williams syndrome.

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9.  Oxytocin receptor activation does not mediate associative fear deficits in a Williams Syndrome model.

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10.  Evidence for associations between Rey-Osterrieth Complex Figure test and motor skill learning in older adults.

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