Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Hannah E. Grosman"'
Autor:
Sylvia B. Guillory, Victoria Z. Baskett, Hannah E. Grosman, Christopher S. McLaughlin, Emily L. Isenstein, Emma Wilkinson, Jordana Weissman, Bari Britvan, M. Pilar Trelles, Danielle B. Halpern, Joseph D. Buxbaum, Paige M. Siper, A. Ting Wang, Alexander Kolevzon, Jennifer H. Foss-Feig
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-11 (2021)
Abstract Background The current study used eye tracking to investigate attention and recognition memory in Phelan-McDermid syndrome (PMS), a rare genetic disorder characterized by intellectual disability, motor delays, and a high likelihood of comorb
Externí odkaz:
https://doaj.org/article/546406152b514a058f00e8e988fa9c1b
Autor:
Emily L. Isenstein, Hannah E. Grosman, Sylvia B. Guillory, Yian Zhang, Sarah Barkley, Christopher S. McLaughlin, Tess Levy, Danielle Halpern, Paige M. Siper, Joseph D. Buxbaum, Alexander Kolevzon, Jennifer H. Foss-Feig
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Phelan-McDermid Syndrome (PMS) is a rare genetic disorder caused by deletion or sequence variation in the SHANK3 gene at terminal chromosome 22 that confers high likelihood of comorbid autism spectrum disorder (ASD). Whereas individuals with idiopath
Externí odkaz:
https://doaj.org/article/974fd2b963194edca691529a84ac36af
Autor:
Emily L. Isenstein, Hannah E. Grosman, Sylvia B. Guillory, Yian Zhang, Sarah Barkley, Christopher S. McLaughlin, Tess Levy, Danielle Halpern, Paige M. Siper, Joseph D. Buxbaum, Alexander Kolevzon, Jennifer H. Foss-Feig
Publikováno v:
Frontiers in neuroscience. 16
Phelan-McDermid Syndrome (PMS) is a rare genetic disorder caused by deletion or sequence variation in theSHANK3gene at terminal chromosome 22 that confers high likelihood of comorbid autism spectrum disorder (ASD). Whereas individuals with idiopathic
Autor:
Sylvia B. Guillory, Victoria Z. Baskett, Hannah E. Grosman, Christopher S. McLaughlin, Emily L. Isenstein, Emma Wilkinson, Jordana Weissman, Bari Britvan, M. Pilar Trelles, Danielle B. Halpern, Joseph D. Buxbaum, Paige M. Siper, A. Ting Wang, Alexander Kolevzon, Jennifer H. Foss-Feig
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-11 (2021)
BackgroundThe current study used eye tracking to investigate attention and recognition memory in Phelan-McDermid syndrome (PMS), a rare genetic disorder characterized by intellectual disability, motor delays, and a high likelihood of comorbid autism