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Cerebral Cortex (New York, N.Y. : 1991)|March 1, 2008
A genetic model for understanding higher order visual processing: functional interactions of the ventral visual stream in Williams syndromeDeepak Sarpal, Bradley R Buchsbaum, Philip D Kohn, et al.
AJNR. American Journal of Neuroradiology|July 23, 2013
Intracranial arteries in individuals with the elastin gene hemideletion of Williams syndromeD P Wint, J A Butman, J C Masdeu, et al.
Orphanet Journal of Rare Diseases|January 7, 2021
Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotypeFarah Qaiser, Yue Yin, Carolyn B Mervis, et al.
Brain : a Journal of Neurology|March 4, 2009
Retinotopically defined primary visual cortex in Williams syndromeRosanna K Olsen, J Shane Kippenhan, Shruti Japee, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 29, 2010
Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndromeHolly H Hobart, Colleen A Morris, Carolyn B Mervis, et al.
Journal of Neurodevelopmental Disorders|March 13, 2022
Patterns and predictors of adaptive skills in 2- to 7-year-old children with Down syndromeEmily K Schworer, Anna J Esbensen, Vivian Nguyen, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Children with 7q11.23 duplication syndrome: psychological characteristicsCarolyn B Mervis, Bonita P Klein-Tasman, Myra J Huffman, et al.
American Journal of Human Genetics|May 15, 2012
Duplication of GTF2I results in separation anxiety in mice and humansCarolyn B Mervis, Joana Dida, Emily Lam, et al.
Brain : a Journal of Neurology|November 6, 2019
Williams syndrome hemideletion and LIMK1 variation both affect dorsal stream functional connectivityMichael D Gregory, Carolyn B Mervis, Maxwell L Elliott, et al.
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