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

L Pavone

Showing results (111-120 of 165) with videos related to

Pageof 17
Sort By:
Annales De Genetique|September 1, 1978
[Partial monosomy 9]L Pavone, F Mollica, G Sorge, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1980
Congenital obstruction of the lacrimal passages in five consecutive generationsF Moro, S Li Volti, S Tomarchio, et al.
American Journal of Medical Genetics|June 1, 1983
Unusual combination of genetic defects in a Sicilian boy: G gamma delta beta thalassemia, G gamma A gamma heterocellular HPFH, beta (0) thalassemia, and albinismG Schilirò, L Pavone, M A Romeo, et al.
Pathologica|May 1, 1979
[A further case of monosomy 9p]L Pavone, F Mollica, G Sorge, et al.
Journal of Pediatric Orthopedics|May 27, 1999
Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1)M Ruggieri, V Pavone, D De Luca, et al.
Pediatric Research|November 1, 1980
Increased erythrocytic spermine in Duchenne muscular dystrophyF Mollica, S Li Volti, A Rapisarda, et al.
Ophthalmic Paediatrics and Genetics|March 1, 1986
Autosomal dominant cone-rod dystrophy associated with sickle-cell trait in a Sicilian familyG Gorgone, S Li Volti, S Tomarchio, et al.
Pediatric Neurology|October 8, 1999
Peripheral lymphocyte subsets and other immune aspects in Rett syndromeA Fiumara, A Sciotto, R Barone, et al.
Clinical Genetics|October 1, 1981
Ocular manifestations in a family with probably X-linked cataractsL Pavone, M La Rosa, G Sorge, et al.
Pediatric Neurology|September 1, 1995
Congenital muscular dystrophies: clinical review and proposed classificationE Parano, L Pavone, A Fiumara, et al.
Pageof 17

Showing results (111-120 of 165) with videos related to

Sort By:
Pageof 17
Annales De Genetique|September 1, 1978
[Partial monosomy 9]L Pavone, F Mollica, G Sorge, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1980
Congenital obstruction of the lacrimal passages in five consecutive generationsF Moro, S Li Volti, S Tomarchio, et al.
American Journal of Medical Genetics|June 1, 1983
Unusual combination of genetic defects in a Sicilian boy: G gamma delta beta thalassemia, G gamma A gamma heterocellular HPFH, beta (0) thalassemia, and albinismG Schilirò, L Pavone, M A Romeo, et al.
Pathologica|May 1, 1979
[A further case of monosomy 9p]L Pavone, F Mollica, G Sorge, et al.
Journal of Pediatric Orthopedics|May 27, 1999
Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1)M Ruggieri, V Pavone, D De Luca, et al.
Pediatric Research|November 1, 1980
Increased erythrocytic spermine in Duchenne muscular dystrophyF Mollica, S Li Volti, A Rapisarda, et al.
Ophthalmic Paediatrics and Genetics|March 1, 1986
Autosomal dominant cone-rod dystrophy associated with sickle-cell trait in a Sicilian familyG Gorgone, S Li Volti, S Tomarchio, et al.
Pediatric Neurology|October 8, 1999
Peripheral lymphocyte subsets and other immune aspects in Rett syndromeA Fiumara, A Sciotto, R Barone, et al.
Clinical Genetics|October 1, 1981
Ocular manifestations in a family with probably X-linked cataractsL Pavone, M La Rosa, G Sorge, et al.
Pediatric Neurology|September 1, 1995
Congenital muscular dystrophies: clinical review and proposed classificationE Parano, L Pavone, A Fiumara, et al.
Pageof 17