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

A Hodgkinson

Showing results (101-110 of 213) with videos related to

Pageof 22
Sort By:
Cell|July 30, 1993
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper proteinC A Hodgkinson, K J Moore, A Nakayama, et al.
The Review of Scientific Instruments|March 3, 2016
Investigation on the electron flux to the wall in the VENUS ion sourceT Thuillier, J Angot, J Y Benitez, et al.
Biological Psychiatry|October 24, 2006
Disrupted in schizophrenia 1 genotype and positive symptoms in schizophreniaPamela DeRosse, Colin A Hodgkinson, Todd Lencz, et al.
American Journal of Medical Genetics|October 1, 1991
Syndrome of mental retardation and distal arthrogryposis in sibsD Chitayat, K A Hodgkinson, S Blaichman, et al.
American Journal of Human Genetics|September 24, 2004
Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorderColin A Hodgkinson, David Goldman, Judith Jaeger, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|April 30, 2016
A Prospective Cohort Study of Influences on Externalizing Behaviors Across Childhood: Results From a Nurse Home Visiting Randomized Controlled TrialMary-Anne Enoch, Harriet Kitzman, Joyce A Smith, et al.
Journal of Medical Genetics|February 28, 2009
Premature death in adults with 22q11.2 deletion syndromeA S Bassett, E W C Chow, J Husted, et al.
Plos One|June 12, 2019
Working memory reflects vulnerability to early life adversity as a risk factor for substance use disorder in the FKBP5 cortisol cochaperone polymorphism, rs9296158William R Lovallo, Ashley Acheson, Andrew J Cohoon, et al.
Neurology|December 25, 2002
A novel form of autosomal recessive pure hereditary spastic paraplegia maps to chromosome 13q14C A Hodgkinson, S Bohlega, S N Abu-Amero, et al.
The Review of Scientific Instruments|March 6, 2014
Production of high intensity 48Ca for the 88-Inch Cyclotron and other updatesJ Y Benitez, K Y Franzen, A Hodgkinson, et al.
Pageof 22

Showing results (101-110 of 213) with videos related to

Sort By:
Pageof 22
Cell|July 30, 1993
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper proteinC A Hodgkinson, K J Moore, A Nakayama, et al.
The Review of Scientific Instruments|March 3, 2016
Investigation on the electron flux to the wall in the VENUS ion sourceT Thuillier, J Angot, J Y Benitez, et al.
Biological Psychiatry|October 24, 2006
Disrupted in schizophrenia 1 genotype and positive symptoms in schizophreniaPamela DeRosse, Colin A Hodgkinson, Todd Lencz, et al.
American Journal of Medical Genetics|October 1, 1991
Syndrome of mental retardation and distal arthrogryposis in sibsD Chitayat, K A Hodgkinson, S Blaichman, et al.
American Journal of Human Genetics|September 24, 2004
Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorderColin A Hodgkinson, David Goldman, Judith Jaeger, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|April 30, 2016
A Prospective Cohort Study of Influences on Externalizing Behaviors Across Childhood: Results From a Nurse Home Visiting Randomized Controlled TrialMary-Anne Enoch, Harriet Kitzman, Joyce A Smith, et al.
Journal of Medical Genetics|February 28, 2009
Premature death in adults with 22q11.2 deletion syndromeA S Bassett, E W C Chow, J Husted, et al.
Plos One|June 12, 2019
Working memory reflects vulnerability to early life adversity as a risk factor for substance use disorder in the FKBP5 cortisol cochaperone polymorphism, rs9296158William R Lovallo, Ashley Acheson, Andrew J Cohoon, et al.
Neurology|December 25, 2002
A novel form of autosomal recessive pure hereditary spastic paraplegia maps to chromosome 13q14C A Hodgkinson, S Bohlega, S N Abu-Amero, et al.
The Review of Scientific Instruments|March 6, 2014
Production of high intensity 48Ca for the 88-Inch Cyclotron and other updatesJ Y Benitez, K Y Franzen, A Hodgkinson, et al.
Pageof 22