Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Eric Legius

Showing results (101-110 of 165) with videos related to

Pageof 17
Sort By:
Human Reproduction (Oxford, England)|November 2, 2018
Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-MAspasia Destouni, Eftychia Dimitriadou, Heleen Masset, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 16, 2017
Emotional and behavioral problems in children and adolescents with neurofibromatosis type 1André B Rietman, Thijs van der Vaart, Ellen Plasschaert, et al.
Acta Neuropathologica|October 31, 2019
NF1 patient missense variants predict a role for ATM in modifying neurofibroma initiationYanan Yu, Kwangmin Choi, Jianqiang Wu, et al.
Genes, Chromosomes & Cancer|December 3, 2009
Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutationsEllen Denayer, Koen Devriendt, Thomy de Ravel, et al.
European Journal of Medical Genetics|February 15, 2020
Next-generation sequencing in prenatal setting: Some examples of unexpected variant associationBerardo Rinaldi, Valerie Race, Anniek Corveleyn, et al.
NPJ Precision Oncology|May 24, 2024
Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variantsRichard Gallon, Carlijn Brekelmans, Marie Martin, et al.
Nature|August 15, 2014
PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapiesThomas De Raedt, Eline Beert, Eric Pasmant, et al.
JAMA Psychiatry|October 21, 2016
Disease Burden and Symptom Structure of Autism in Neurofibromatosis Type 1: A Study of the International NF1-ASD Consortium Team (INFACT)Stephanie M Morris, Maria T Acosta, Shruti Garg, et al.
The Lancet. Neurology|October 5, 2013
Simvastatin for cognitive deficits and behavioural problems in patients with neurofibromatosis type 1 (NF1-SIMCODA): a randomised, placebo-controlled trialThijs van der Vaart, Ellen Plasschaert, André B Rietman, et al.
Journal of the National Cancer Institute|November 9, 2017
Neurofibromatosis Type 1-Associated MPNST State of the Science: Outlining a Research Agenda for the FutureKarlyne M Reilly, AeRang Kim, Jaishri Blakely, et al.
Pageof 17

Showing results (101-110 of 165) with videos related to

Sort By:
Pageof 17
Human Reproduction (Oxford, England)|November 2, 2018
Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-MAspasia Destouni, Eftychia Dimitriadou, Heleen Masset, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 16, 2017
Emotional and behavioral problems in children and adolescents with neurofibromatosis type 1André B Rietman, Thijs van der Vaart, Ellen Plasschaert, et al.
Acta Neuropathologica|October 31, 2019
NF1 patient missense variants predict a role for ATM in modifying neurofibroma initiationYanan Yu, Kwangmin Choi, Jianqiang Wu, et al.
Genes, Chromosomes & Cancer|December 3, 2009
Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutationsEllen Denayer, Koen Devriendt, Thomy de Ravel, et al.
European Journal of Medical Genetics|February 15, 2020
Next-generation sequencing in prenatal setting: Some examples of unexpected variant associationBerardo Rinaldi, Valerie Race, Anniek Corveleyn, et al.
NPJ Precision Oncology|May 24, 2024
Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variantsRichard Gallon, Carlijn Brekelmans, Marie Martin, et al.
Nature|August 15, 2014
PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapiesThomas De Raedt, Eline Beert, Eric Pasmant, et al.
JAMA Psychiatry|October 21, 2016
Disease Burden and Symptom Structure of Autism in Neurofibromatosis Type 1: A Study of the International NF1-ASD Consortium Team (INFACT)Stephanie M Morris, Maria T Acosta, Shruti Garg, et al.
The Lancet. Neurology|October 5, 2013
Simvastatin for cognitive deficits and behavioural problems in patients with neurofibromatosis type 1 (NF1-SIMCODA): a randomised, placebo-controlled trialThijs van der Vaart, Ellen Plasschaert, André B Rietman, et al.
Journal of the National Cancer Institute|November 9, 2017
Neurofibromatosis Type 1-Associated MPNST State of the Science: Outlining a Research Agenda for the FutureKarlyne M Reilly, AeRang Kim, Jaishri Blakely, et al.
Pageof 17