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F Bonnet-Brilhault

Showing results (21-30 of 26) with videos related to

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American Journal of Medical Genetics|July 23, 1998
Anticipation in schizophrenia: no evidence of expanded CAG/CTG repeat sequences in French families and sporadic casesC Laurent, C Zander, F Thibaut, et al.
Molecular Psychiatry|June 10, 2015
GABA/Glutamate synaptic pathways targeted by integrative genomic and electrophysiological explorations distinguish autism from intellectual disabilityF Bonnet-Brilhault, S Alirol, R Blanc, et al.
Molecular Syndromology|April 10, 2014
Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 DeletionsC Dubourg, F Bonnet-Brilhault, A Toutain, et al.
Behavior Genetics|January 12, 2013
Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French familiesM Huc-Chabrolle, C Charon, A Guilmatre, et al.
Journal of Autism and Developmental Disorders|February 23, 2018
Evaluating Sex and Age Differences in ADI-R and ADOS Scores in a Large European Multi-site Sample of Individuals with Autism Spectrum DisorderJ Tillmann, K Ashwood, M Absoud, et al.
Social Psychiatry and Psychiatric Epidemiology|February 11, 2022
Demographic, clinical, and service-use characteristics related to the clinician's recommendation to transition from child to adult mental health servicesS E Gerritsen, L S van Bodegom, G C Dieleman, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
American Journal of Medical Genetics|July 23, 1998
Anticipation in schizophrenia: no evidence of expanded CAG/CTG repeat sequences in French families and sporadic casesC Laurent, C Zander, F Thibaut, et al.
Molecular Psychiatry|June 10, 2015
GABA/Glutamate synaptic pathways targeted by integrative genomic and electrophysiological explorations distinguish autism from intellectual disabilityF Bonnet-Brilhault, S Alirol, R Blanc, et al.
Molecular Syndromology|April 10, 2014
Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 DeletionsC Dubourg, F Bonnet-Brilhault, A Toutain, et al.
Behavior Genetics|January 12, 2013
Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French familiesM Huc-Chabrolle, C Charon, A Guilmatre, et al.
Journal of Autism and Developmental Disorders|February 23, 2018
Evaluating Sex and Age Differences in ADI-R and ADOS Scores in a Large European Multi-site Sample of Individuals with Autism Spectrum DisorderJ Tillmann, K Ashwood, M Absoud, et al.
Social Psychiatry and Psychiatric Epidemiology|February 11, 2022
Demographic, clinical, and service-use characteristics related to the clinician's recommendation to transition from child to adult mental health servicesS E Gerritsen, L S van Bodegom, G C Dieleman, et al.
Pageof 3