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

V Briscioli

Showing results (1-10 of 15) with videos related to

Pageof 2
Sort By:
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1993
[Syndromes in outpatient experience]F Lalatta, A Selicorni, V Briscioli
American Journal of Medical Genetics|January 20, 1997
Malignant melanoma and Charcot-Marie-Tooth disease: a further caseS Manoukian, V Briscioli, F Lalatta
American Journal of Medical Genetics|July 31, 1995
Kaufman oculocerebrofacial syndrome in a girl of 15 yearsV Briscioli, S Manoukian, A Selicorni, et al.
American Journal of Medical Genetics|August 22, 1997
Thomas syndrome: clinical variability and autosomal recessive inheritanceV Briscioli, F Lalatta, T Rizzuti, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 1, 1996
[Odontochondrodysplasia]P Maroteaux, V Briscioli, F Lalatta, et al.
Clinical Genetics|November 1, 1994
A de novo 6q11-q15 duplication investigated by chromosome paintingD Giardino, N Rizzi, V Briscioli, et al.
Journal of Neurology|June 9, 1998
A new non-radioactive method for the screening and prenatal diagnosis of myotonic dystrophy patientsR Brugnoni, L Morandi, B Brambati, et al.
Journal of Medical Genetics|July 1, 1993
Trisomy 10qter confirmed by in situ hybridisationV Briscioli, G Floridia, E Rossi, et al.
Clinical Genetics|November 27, 1998
An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutationS Russo, V Briscioli, F Cogliati, et al.
European Journal of Human Genetics : EJHG|February 13, 2002
Cryptic subtelomeric translocation t(2;16)(q37;q24) segregating in a family with unexplained stillbirths and a dysmorphic, slightly retarded childD Giardino, P Finelli, G Gottardi, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1993
[Syndromes in outpatient experience]F Lalatta, A Selicorni, V Briscioli
American Journal of Medical Genetics|January 20, 1997
Malignant melanoma and Charcot-Marie-Tooth disease: a further caseS Manoukian, V Briscioli, F Lalatta
American Journal of Medical Genetics|July 31, 1995
Kaufman oculocerebrofacial syndrome in a girl of 15 yearsV Briscioli, S Manoukian, A Selicorni, et al.
American Journal of Medical Genetics|August 22, 1997
Thomas syndrome: clinical variability and autosomal recessive inheritanceV Briscioli, F Lalatta, T Rizzuti, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 1, 1996
[Odontochondrodysplasia]P Maroteaux, V Briscioli, F Lalatta, et al.
Clinical Genetics|November 1, 1994
A de novo 6q11-q15 duplication investigated by chromosome paintingD Giardino, N Rizzi, V Briscioli, et al.
Journal of Neurology|June 9, 1998
A new non-radioactive method for the screening and prenatal diagnosis of myotonic dystrophy patientsR Brugnoni, L Morandi, B Brambati, et al.
Journal of Medical Genetics|July 1, 1993
Trisomy 10qter confirmed by in situ hybridisationV Briscioli, G Floridia, E Rossi, et al.
Clinical Genetics|November 27, 1998
An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutationS Russo, V Briscioli, F Cogliati, et al.
European Journal of Human Genetics : EJHG|February 13, 2002
Cryptic subtelomeric translocation t(2;16)(q37;q24) segregating in a family with unexplained stillbirths and a dysmorphic, slightly retarded childD Giardino, P Finelli, G Gottardi, et al.
Pageof 2