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 Sebastio

Showing results (21-30 of 67) with videos related to

Pageof 7
Sort By:
European Journal of Ophthalmology|October 13, 2007
Incidence of ocular pathologies in Italian children with Down syndromeF Fimiani, A Iovine, R Carelli, et al.
Minerva Pediatrica|September 22, 1976
[Patau's syndrome with single mosaicism: 46,XY,13-,t(13p13p)+46,XY,13-,t(13p13p)+ or 46,XY,13-,(13p13p) and 46,Xy,13-,(13q13q)]V Ventruto, L Di Palma, B Festa, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1982
[Efficacy of dietetic treatment in a case of galactosemia diagnosed late]G Sebastio, F Albini, L di Martino, et al.
Human Genetics|March 1, 1992
Lung involvement, the delta F508 mutation and DNA haplotype analysis in cystic fibrosisF Santamaria, D Salvatore, O Castiglione, et al.
Journal of Medical Genetics|October 1, 1976
Family study of inherited syndrome with multiple congenital deformities: symphalangism, carpal and tarsal fusion, brachydactyly, craniosynostosis, strabismus, hip osteochondritisV Ventruto, R Di Girlamo, B Festa, et al.
American Journal of Medical Genetics|October 16, 1996
Congenital Alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency in two sibsC Pignata, M Fiore, V Guzzetta, et al.
The Journal of Pediatrics|February 1, 1995
Lysinuric protein intolerance characterized by bone marrow abnormalities and severe clinical courseG Parenti, G Sebastio, P Strisciuglio, et al.
Biochemical and Biophysical Research Communications|December 16, 1987
The biosynthesis of intestinal sucrase-isomaltase in human embryo is most likely controlled at the level of transcriptionG Sebastio, W Hunziker, B O'Neill, et al.
American Journal of Medical Genetics|August 10, 1999
Geleophysic dysplasia: 7-year follow-up study of a patient with an intermediate formL Titomanlio, R Della Casa, M Lecora, et al.
Journal of Medical Genetics|October 1, 1977
Leprechaunism with mosaicism 46, XX/47, XX extra ring chromosomeV Ventruto, L Sebastio, G Sebastio, et al.
Pageof 7

Showing results (21-30 of 67) with videos related to

Sort By:
Pageof 7
European Journal of Ophthalmology|October 13, 2007
Incidence of ocular pathologies in Italian children with Down syndromeF Fimiani, A Iovine, R Carelli, et al.
Minerva Pediatrica|September 22, 1976
[Patau's syndrome with single mosaicism: 46,XY,13-,t(13p13p)+46,XY,13-,t(13p13p)+ or 46,XY,13-,(13p13p) and 46,Xy,13-,(13q13q)]V Ventruto, L Di Palma, B Festa, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1982
[Efficacy of dietetic treatment in a case of galactosemia diagnosed late]G Sebastio, F Albini, L di Martino, et al.
Human Genetics|March 1, 1992
Lung involvement, the delta F508 mutation and DNA haplotype analysis in cystic fibrosisF Santamaria, D Salvatore, O Castiglione, et al.
Journal of Medical Genetics|October 1, 1976
Family study of inherited syndrome with multiple congenital deformities: symphalangism, carpal and tarsal fusion, brachydactyly, craniosynostosis, strabismus, hip osteochondritisV Ventruto, R Di Girlamo, B Festa, et al.
American Journal of Medical Genetics|October 16, 1996
Congenital Alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency in two sibsC Pignata, M Fiore, V Guzzetta, et al.
The Journal of Pediatrics|February 1, 1995
Lysinuric protein intolerance characterized by bone marrow abnormalities and severe clinical courseG Parenti, G Sebastio, P Strisciuglio, et al.
Biochemical and Biophysical Research Communications|December 16, 1987
The biosynthesis of intestinal sucrase-isomaltase in human embryo is most likely controlled at the level of transcriptionG Sebastio, W Hunziker, B O'Neill, et al.
American Journal of Medical Genetics|August 10, 1999
Geleophysic dysplasia: 7-year follow-up study of a patient with an intermediate formL Titomanlio, R Della Casa, M Lecora, et al.
Journal of Medical Genetics|October 1, 1977
Leprechaunism with mosaicism 46, XX/47, XX extra ring chromosomeV Ventruto, L Sebastio, G Sebastio, et al.
Pageof 7