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 Del Porto

Showing results (1-10 of 57) with videos related to

Pageof 6
Sort By:
Minerva Pediatrica|March 1, 1988
[Review of the Pena-Shokeir syndrome I, Pena-Shokeir II and Neu-Laxova. Clinical and interpretative contribution]N Sulli, G del Porto
Acta Geneticae Medicae Et Gemellologiae|January 1, 1973
Sweat electrolytes as a clinical and genetic test in mucoviscidosis. Study of variability and genetic conditioningG Del Porto, B Di Tonto
Cardiologia (Rome, Italy)|December 1, 1991
[Hyperlipidemia, blood coagulation factors, hereditary familial factors and coronary atherosclerosis]M Penco, G Del Porto, A Dagianti
Quaderni Sclavo Di Diagnostica Clinica E Di Laboratorio|March 1, 1971
[Enzyme genetics]L Gedda, G Del Porto, G Brenci
Acta Geneticae Medicae Et Gemellologiae|January 1, 1970
[Malformations in man: a twin study]G Del Porto, A Del Porto-Mercuri
Acta Geneticae Medicae Et Gemellologiae|January 1, 1970
Genetic criteria for the classification of malformations--a twin studyL Gedda, G Del Porto, M T Lun
Minerva Ginecologica|January 1, 1986
[Complex balanced translation]G Del Porto, P Grammatico, M Baldi, et al.
Minerva Ginecologica|December 1, 1985
[Transferrin and infertility: genetic-clinical study. Preliminary note]G Del Porto, R Donnini, M Baldi, et al.
Annals of the New York Academy of Sciences|November 21, 1992
Cytogenetic and DNA repair studies in a patient affected by the neonatal progeroid syndromeL Chessa, V Bastianon, G Del Porto, et al.
Disease Markers|May 1, 1990
Xeroderma pigmentosum: clonal chromosomal rearrangements in a pre-cancerous skin lesionL Chessa, F Nuzzo, M Stefanini, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
Minerva Pediatrica|March 1, 1988
[Review of the Pena-Shokeir syndrome I, Pena-Shokeir II and Neu-Laxova. Clinical and interpretative contribution]N Sulli, G del Porto
Acta Geneticae Medicae Et Gemellologiae|January 1, 1973
Sweat electrolytes as a clinical and genetic test in mucoviscidosis. Study of variability and genetic conditioningG Del Porto, B Di Tonto
Cardiologia (Rome, Italy)|December 1, 1991
[Hyperlipidemia, blood coagulation factors, hereditary familial factors and coronary atherosclerosis]M Penco, G Del Porto, A Dagianti
Quaderni Sclavo Di Diagnostica Clinica E Di Laboratorio|March 1, 1971
[Enzyme genetics]L Gedda, G Del Porto, G Brenci
Acta Geneticae Medicae Et Gemellologiae|January 1, 1970
[Malformations in man: a twin study]G Del Porto, A Del Porto-Mercuri
Acta Geneticae Medicae Et Gemellologiae|January 1, 1970
Genetic criteria for the classification of malformations--a twin studyL Gedda, G Del Porto, M T Lun
Minerva Ginecologica|January 1, 1986
[Complex balanced translation]G Del Porto, P Grammatico, M Baldi, et al.
Minerva Ginecologica|December 1, 1985
[Transferrin and infertility: genetic-clinical study. Preliminary note]G Del Porto, R Donnini, M Baldi, et al.
Annals of the New York Academy of Sciences|November 21, 1992
Cytogenetic and DNA repair studies in a patient affected by the neonatal progeroid syndromeL Chessa, V Bastianon, G Del Porto, et al.
Disease Markers|May 1, 1990
Xeroderma pigmentosum: clonal chromosomal rearrangements in a pre-cancerous skin lesionL Chessa, F Nuzzo, M Stefanini, et al.
Pageof 6