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

G Novelli

Showing results (111-120 of 330) with videos related to

Pageof 33
Sort By:
Mutation Research|July 24, 2001
Three novel mutations causing a truncated protein within the RP2 gene in Italian families with X-linked retinitis pigmentosaA De Luca, I Torrente, M Mangino, et al.
Human Mutation|January 1, 1993
Molecular characterization of a frameshift mutation in exon 19 of the CFTR geneF Sangiuolo, S Lo Cicero, P Maceratesi, et al.
Prenatal Diagnosis|June 1, 1994
First-trimester prenatal diagnosis of spinal muscular atrophy using microsatellite markersS Lo Cicero, F Capon, S Melchionda, et al.
Human Mutation|January 1, 1994
North Eurasian origin of the myotonic dystrophy mutationG Novelli, G Spedini, G Destro-Bisol, et al.
Human Heredity|December 22, 1998
A novel mutation (R271X) in the myotubularin gene causes a severe miotubular myopathyA De Luca, I Torrente, M Mangino, et al.
Minerva Ginecologica|April 1, 1981
[Effect of treatment with oral 6-methyl-17-hydroxyprogesterone acetate in endometrial adenocarcinoma. Histochemical and ultrastructural aspects]G Vecchietti, G Gerzeli, L Zanoio, et al.
Human Genetics|December 1, 1994
Exclusion of linkage with chromosome 21 in families with recurrence of non-Down's atrioventricular canalM Gennarelli, G Novelli, M C Digilio, et al.
Human Genetics|September 1, 1990
Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF familiesG Novelli, P Gasparini, A Savoia, et al.
Journal of Human Genetics|February 4, 1999
A single-nucleotide polymorphism in the human bone morphogenetic protein-4 (BMP 4) geneM Mangino, I Torrente, A De Luca, et al.
Clinical Genetics|March 23, 2004
Paternal origin of LMNA mutations in Hutchinson-Gilford progeriaM R D'Apice, R Tenconi, I Mammi, et al.
Pageof 33

Showing results (111-120 of 330) with videos related to

Sort By:
Pageof 33
Mutation Research|July 24, 2001
Three novel mutations causing a truncated protein within the RP2 gene in Italian families with X-linked retinitis pigmentosaA De Luca, I Torrente, M Mangino, et al.
Human Mutation|January 1, 1993
Molecular characterization of a frameshift mutation in exon 19 of the CFTR geneF Sangiuolo, S Lo Cicero, P Maceratesi, et al.
Prenatal Diagnosis|June 1, 1994
First-trimester prenatal diagnosis of spinal muscular atrophy using microsatellite markersS Lo Cicero, F Capon, S Melchionda, et al.
Human Mutation|January 1, 1994
North Eurasian origin of the myotonic dystrophy mutationG Novelli, G Spedini, G Destro-Bisol, et al.
Human Heredity|December 22, 1998
A novel mutation (R271X) in the myotubularin gene causes a severe miotubular myopathyA De Luca, I Torrente, M Mangino, et al.
Minerva Ginecologica|April 1, 1981
[Effect of treatment with oral 6-methyl-17-hydroxyprogesterone acetate in endometrial adenocarcinoma. Histochemical and ultrastructural aspects]G Vecchietti, G Gerzeli, L Zanoio, et al.
Human Genetics|December 1, 1994
Exclusion of linkage with chromosome 21 in families with recurrence of non-Down's atrioventricular canalM Gennarelli, G Novelli, M C Digilio, et al.
Human Genetics|September 1, 1990
Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF familiesG Novelli, P Gasparini, A Savoia, et al.
Journal of Human Genetics|February 4, 1999
A single-nucleotide polymorphism in the human bone morphogenetic protein-4 (BMP 4) geneM Mangino, I Torrente, A De Luca, et al.
Clinical Genetics|March 23, 2004
Paternal origin of LMNA mutations in Hutchinson-Gilford progeriaM R D'Apice, R Tenconi, I Mammi, et al.
Pageof 33