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Matthew Hunter

Showing results (11-20 of 30) with videos related to

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BMJ Paediatrics Open|October 6, 2025
Towards an agreed approach to investigate children with developmental regressionKirsten Furley, Matthew Hunter, Gauravi Gawade, et al.
American Journal of Medical Genetics. Part A|May 7, 2015
A familial 7q36.3 duplication associated with agenesis of the corpus callosumKeith Wong, Randal Moldrich, Matthew Hunter, et al.
Epilepsy & Behavior : E&B|December 5, 2018
Analysis of EEG networks and their correlation with cognitive impairment in preschool children with epilepsyEli Kinney-Lang, Michael Yoong, Matthew Hunter, et al.
Journal of Food Protection|August 2, 2025
Paralytic Shellfish Poisoning Outbreak-Oregon, United States, 2024Rosalie T Trevejo, Matthew Hunter, Terran Gilbreath, et al.
Epilepsy & Behavior : E&B|February 10, 2018
Cognitive impairment in early onset epilepsy is associated with reduced left thalamic volumeMichael Yoong, Matthew Hunter, Jacqueline Stephen, et al.
Genes|June 9, 2018
Prenatal Diagnosis of Fragile X Syndrome in a Twin Pregnancy Complicated by a Complete RetractionYael Prawer, Matthew Hunter, Sara Cronin, et al.
American Journal of Medical Genetics. Part A|January 11, 2013
Maternal attitudes to newborn screening for fragile X syndromeLouise Christie, Tiffany Wotton, Bruce Bennetts, et al.
American Journal of Medical Genetics. Part A|October 4, 2016
Partially methylated alleles, microdeletion, and tissue mosaicism in a fragile X male with tremor and ataxia at 30 years of age: A case reportYun Tae Hwang, Solange Mabel Aliaga, Marta Arpone, et al.
European Journal of Human Genetics : EJHG|September 4, 2020
Wilms tumor in patients with osteopathia striata with cranial sclerosisAlicia Bach, Jingyi Mi, Matthew Hunter, et al.
Frontiers in Dementia|July 31, 2024
Remote data collection speech analysis in people at risk for Alzheimer's disease dementia: usability and acceptability resultsSarah Gregory, John Harrison, Janna Herrmann, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
BMJ Paediatrics Open|October 6, 2025
Towards an agreed approach to investigate children with developmental regressionKirsten Furley, Matthew Hunter, Gauravi Gawade, et al.
American Journal of Medical Genetics. Part A|May 7, 2015
A familial 7q36.3 duplication associated with agenesis of the corpus callosumKeith Wong, Randal Moldrich, Matthew Hunter, et al.
Epilepsy & Behavior : E&B|December 5, 2018
Analysis of EEG networks and their correlation with cognitive impairment in preschool children with epilepsyEli Kinney-Lang, Michael Yoong, Matthew Hunter, et al.
Journal of Food Protection|August 2, 2025
Paralytic Shellfish Poisoning Outbreak-Oregon, United States, 2024Rosalie T Trevejo, Matthew Hunter, Terran Gilbreath, et al.
Epilepsy & Behavior : E&B|February 10, 2018
Cognitive impairment in early onset epilepsy is associated with reduced left thalamic volumeMichael Yoong, Matthew Hunter, Jacqueline Stephen, et al.
Genes|June 9, 2018
Prenatal Diagnosis of Fragile X Syndrome in a Twin Pregnancy Complicated by a Complete RetractionYael Prawer, Matthew Hunter, Sara Cronin, et al.
American Journal of Medical Genetics. Part A|January 11, 2013
Maternal attitudes to newborn screening for fragile X syndromeLouise Christie, Tiffany Wotton, Bruce Bennetts, et al.
American Journal of Medical Genetics. Part A|October 4, 2016
Partially methylated alleles, microdeletion, and tissue mosaicism in a fragile X male with tremor and ataxia at 30 years of age: A case reportYun Tae Hwang, Solange Mabel Aliaga, Marta Arpone, et al.
European Journal of Human Genetics : EJHG|September 4, 2020
Wilms tumor in patients with osteopathia striata with cranial sclerosisAlicia Bach, Jingyi Mi, Matthew Hunter, et al.
Frontiers in Dementia|July 31, 2024
Remote data collection speech analysis in people at risk for Alzheimer's disease dementia: usability and acceptability resultsSarah Gregory, John Harrison, Janna Herrmann, et al.
Pageof 3