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Brenda Finucane

Showing results (21-30 of 28) with videos related to

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Journal of Genetic Counseling|May 15, 2007
Recommendations from multi-disciplinary focus groups on cascade testing and genetic counseling for fragile X-associated disordersAllyn McConkie-Rosell, Liane Abrams, Brenda Finucane, et al.
Journal of Neurodevelopmental Disorders|August 12, 2014
AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmissionCarolyn M Yrigollen, Loreto Martorell, Blythe Durbin-Johnson, et al.
Pediatrics|November 7, 2012
Newborn, carrier, and early childhood screening recommendations for fragile XLiane Abrams, Amy Cronister, William T Brown, et al.
Epilepsia|February 8, 2014
A survey of seizures and current treatments in 15q duplication syndromeKerry D Conant, Brenda Finucane, Nicole Cleary, et al.
Genes|January 21, 2023
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease ResearchLauren K White, T Blaine Crowley, Brenda Finucane, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 10, 2007
Fragile X-associated tremor/ataxia syndrome: clinical features, genetics, and testing guidelinesElizabeth Berry-Kravis, Liane Abrams, Sarah M Coffey, et al.
American Journal of Human Genetics|October 13, 2006
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaLars Feuk, Aino Kalervo, Marita Lipsanen-Nyman, et al.
The American Journal of Psychiatry|March 3, 2022
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and PsychopathologySébastien Jacquemont, Guillaume Huguet, Marieke Klein, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Journal of Genetic Counseling|May 15, 2007
Recommendations from multi-disciplinary focus groups on cascade testing and genetic counseling for fragile X-associated disordersAllyn McConkie-Rosell, Liane Abrams, Brenda Finucane, et al.
Journal of Neurodevelopmental Disorders|August 12, 2014
AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmissionCarolyn M Yrigollen, Loreto Martorell, Blythe Durbin-Johnson, et al.
Pediatrics|November 7, 2012
Newborn, carrier, and early childhood screening recommendations for fragile XLiane Abrams, Amy Cronister, William T Brown, et al.
Epilepsia|February 8, 2014
A survey of seizures and current treatments in 15q duplication syndromeKerry D Conant, Brenda Finucane, Nicole Cleary, et al.
Genes|January 21, 2023
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease ResearchLauren K White, T Blaine Crowley, Brenda Finucane, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 10, 2007
Fragile X-associated tremor/ataxia syndrome: clinical features, genetics, and testing guidelinesElizabeth Berry-Kravis, Liane Abrams, Sarah M Coffey, et al.
American Journal of Human Genetics|October 13, 2006
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaLars Feuk, Aino Kalervo, Marita Lipsanen-Nyman, et al.
The American Journal of Psychiatry|March 3, 2022
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and PsychopathologySébastien Jacquemont, Guillaume Huguet, Marieke Klein, et al.
Pageof 3