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

O Zuffardi

Showing results (31-40 of 159) with videos related to

Pageof 16
Sort By:
Genomics|September 1, 1994
Molecular cloning of cDNAs encoding human carnitine acetyltransferase and mapping of the corresponding gene to chromosome 9q34.1O Corti, G Finocchiaro, E Rossi, et al.
Journal of Medical Genetics|August 1, 1977
15/15 translocation in Prader-Willi syndromeM Fraccaro, O Zuffardi, E M Buhler, et al.
Human Genetics|February 1, 1992
The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyteP Simi, M Ceccarelli, A Barachini, et al.
European Journal of Medical Genetics|June 15, 2007
A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's linesG Gimelli, R Giorda, S Beri, et al.
Chromosoma|September 28, 2000
CENP-G in neocentromeres and inactive centromeresG Gimelli, O Zuffardi, S Giglio, et al.
Human Genetics|May 1, 1992
Evidence for an ancestral alphoid domain on the long arm of human chromosome 2R Avarello, A Pedicini, A Caiulo, et al.
Human Genetics|February 1, 1980
Trisomy 16q21 = to qterA Garau, G Crisponi, D Peretti, et al.
Genomics|October 1, 1991
Probe St35-239 (DXYS64) reveals homology between the distal ends of Xq and YqA Pedicini, G Camerino, R Avarello, et al.
Human Genetics|August 1, 1988
A dominantly inherited syndrome (microcephaly, short stature, peculiar facies, mental retardation) associated with two balanced rearrangements involving chromosomes 2;7 and 5;20R Vivarelli, O Zuffardi, P Maraschio, et al.
Human Genetics|May 1, 1986
Indirect immunofluorescence of inactive centromeres as indicator of centromeric functionD Peretti, P Maraschio, S Lambiase, et al.
Pageof 16

Showing results (31-40 of 159) with videos related to

Sort By:
Pageof 16
Genomics|September 1, 1994
Molecular cloning of cDNAs encoding human carnitine acetyltransferase and mapping of the corresponding gene to chromosome 9q34.1O Corti, G Finocchiaro, E Rossi, et al.
Journal of Medical Genetics|August 1, 1977
15/15 translocation in Prader-Willi syndromeM Fraccaro, O Zuffardi, E M Buhler, et al.
Human Genetics|February 1, 1992
The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyteP Simi, M Ceccarelli, A Barachini, et al.
European Journal of Medical Genetics|June 15, 2007
A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's linesG Gimelli, R Giorda, S Beri, et al.
Chromosoma|September 28, 2000
CENP-G in neocentromeres and inactive centromeresG Gimelli, O Zuffardi, S Giglio, et al.
Human Genetics|May 1, 1992
Evidence for an ancestral alphoid domain on the long arm of human chromosome 2R Avarello, A Pedicini, A Caiulo, et al.
Human Genetics|February 1, 1980
Trisomy 16q21 = to qterA Garau, G Crisponi, D Peretti, et al.
Genomics|October 1, 1991
Probe St35-239 (DXYS64) reveals homology between the distal ends of Xq and YqA Pedicini, G Camerino, R Avarello, et al.
Human Genetics|August 1, 1988
A dominantly inherited syndrome (microcephaly, short stature, peculiar facies, mental retardation) associated with two balanced rearrangements involving chromosomes 2;7 and 5;20R Vivarelli, O Zuffardi, P Maraschio, et al.
Human Genetics|May 1, 1986
Indirect immunofluorescence of inactive centromeres as indicator of centromeric functionD Peretti, P Maraschio, S Lambiase, et al.
Pageof 16