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 Ciccodicola

Showing results (21-30 of 47) with videos related to

Pageof 5
Sort By:
Genomics|November 1, 1994
YAC contig organization and CpG island analysis in Xq28G Palmieri, G Romano, A Ciccodicola, et al.
Genomics|July 1, 1991
Sequence of human glucose-6-phosphate dehydrogenase cloned in plasmids and a yeast artificial chromosomeE Y Chen, A Cheng, A Lee, et al.
Neuroscience|July 18, 2008
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformationsF Gianfrancesco, T Esposito, S Penco, et al.
American Journal of Human Genetics|May 1, 1988
An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequenceM D'Urso, L Luzzatto, L Perroni, et al.
Human Molecular Genetics|October 1, 1995
Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the diseaseS Bione, K Small, V M Aksmanovic, et al.
Nature Genetics|August 10, 2000
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosaR Vervoort, A Lennon, A C Bird, et al.
Human Molecular Genetics|May 1, 1996
Long-range sequence analysis in Xq28: thirteen known and six candidate genes in 219.4 kb of high GC DNA between the RCP/GCP and G6PD lociE Y Chen, M Zollo, R Mazzarella, et al.
The British Journal of Ophthalmology|August 21, 2003
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian familiesF Simonelli, G Cennamo, C Ziviello, et al.
Gene|March 18, 1997
Expressed STSs and transcription of human Xq28T Esposito, A Ciccodicola, L Flagiello, et al.
Human Molecular Genetics|November 16, 2001
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genesS Aradhya, T Bardaro, P Galgóczy, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Genomics|November 1, 1994
YAC contig organization and CpG island analysis in Xq28G Palmieri, G Romano, A Ciccodicola, et al.
Genomics|July 1, 1991
Sequence of human glucose-6-phosphate dehydrogenase cloned in plasmids and a yeast artificial chromosomeE Y Chen, A Cheng, A Lee, et al.
Neuroscience|July 18, 2008
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformationsF Gianfrancesco, T Esposito, S Penco, et al.
American Journal of Human Genetics|May 1, 1988
An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequenceM D'Urso, L Luzzatto, L Perroni, et al.
Human Molecular Genetics|October 1, 1995
Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the diseaseS Bione, K Small, V M Aksmanovic, et al.
Nature Genetics|August 10, 2000
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosaR Vervoort, A Lennon, A C Bird, et al.
Human Molecular Genetics|May 1, 1996
Long-range sequence analysis in Xq28: thirteen known and six candidate genes in 219.4 kb of high GC DNA between the RCP/GCP and G6PD lociE Y Chen, M Zollo, R Mazzarella, et al.
The British Journal of Ophthalmology|August 21, 2003
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian familiesF Simonelli, G Cennamo, C Ziviello, et al.
Gene|March 18, 1997
Expressed STSs and transcription of human Xq28T Esposito, A Ciccodicola, L Flagiello, et al.
Human Molecular Genetics|November 16, 2001
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genesS Aradhya, T Bardaro, P Galgóczy, et al.
Pageof 5