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

L D'Agruma

Showing results (11-20 of 15) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 15 results.
European Journal of Human Genetics : EJHG|October 22, 1998
Generation of a transcription map of a 1 Mbase region containing the HFE gene (6p22)A Totaro, A Roetto, J M Rommens, et al.
Human Molecular Genetics|September 1, 1997
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in MediterraneansL Zelante, P Gasparini, X Estivill, et al.
Molecular Psychiatry|July 20, 2005
Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactionsM D'Amelio, I Ricci, R Sacco, et al.
Psychiatric Genetics|May 29, 2004
Enhanced APOE2 transmission rates in families with autistic probandsA M Persico, L D'Agruma, L Zelante, et al.
Molecular Psychiatry|April 24, 2001
Reelin gene alleles and haplotypes as a factor predisposing to autistic disorderA M Persico, L D'Agruma, N Maiorano, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
European Journal of Human Genetics : EJHG|October 22, 1998
Generation of a transcription map of a 1 Mbase region containing the HFE gene (6p22)A Totaro, A Roetto, J M Rommens, et al.
Human Molecular Genetics|September 1, 1997
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in MediterraneansL Zelante, P Gasparini, X Estivill, et al.
Molecular Psychiatry|July 20, 2005
Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactionsM D'Amelio, I Ricci, R Sacco, et al.
Psychiatric Genetics|May 29, 2004
Enhanced APOE2 transmission rates in families with autistic probandsA M Persico, L D'Agruma, L Zelante, et al.
Molecular Psychiatry|April 24, 2001
Reelin gene alleles and haplotypes as a factor predisposing to autistic disorderA M Persico, L D'Agruma, N Maiorano, et al.
Pageof 2