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 Dalprà

Showing results (1-10 of 64) with videos related to

Pageof 7
Sort By:
Human Genetics|January 1, 1980
A duplication-deficiency X chromosome in a girl with severe mental retardationN Sacchi, L Dalprà, E Kehyayan
Chromosoma|January 10, 1998
Expression of three rare fragile sites: chromosomal truncation, amplification of distal segment and telomeric renewalN Villa, L Dalprà, L Larizza
Pathologica|May 1, 1979
[Use of chromosomal variants for determination of paternity]G Morganti, L Dalprà, L De Carli
Strabismus|February 15, 2011
Brown's syndrome associated with Smith-Magenis syndrome: Case reportR Salati, G Marini, A Degiuli, et al.
Annales De Genetique|January 1, 1996
Further delineation of 7p trisomy. Case report and review of literatureR Pallotta, L Dalprà, P Fusilli, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1985
[Spondylocostal dysostosis]G Bonora, D Baronciani, G Gargantini, et al.
Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia|September 1, 1988
[Dominant epidermolysis bullosa dystrophica of Cockayne-Touraine. Presentation of a familial case and cytogenetic investigation]P Amerio, R Pallotta, D Di Donato, et al.
Minerva Pediatrica|February 28, 1986
[Partial trisomy 9q: comparison of the syndrome in 2 sisters]G P Bianchi, P Cantone, L Dalprà, et al.
Annales De Genetique|January 1, 1993
Prenatal diagnosis of an extranumerary i(22p) with normal phenotypeL Doneda, L Dalprà, M G Tibiletti, et al.
Journal of Medical Genetics|September 19, 2000
Monosomy and trisomy 1q44-qter in two sisters originating from a half cryptic 1q;15p translocationN Villa, E Sala, D Colombo, et al.
Pageof 7

Showing results (1-10 of 64) with videos related to

Sort By:
Pageof 7
Human Genetics|January 1, 1980
A duplication-deficiency X chromosome in a girl with severe mental retardationN Sacchi, L Dalprà, E Kehyayan
Chromosoma|January 10, 1998
Expression of three rare fragile sites: chromosomal truncation, amplification of distal segment and telomeric renewalN Villa, L Dalprà, L Larizza
Pathologica|May 1, 1979
[Use of chromosomal variants for determination of paternity]G Morganti, L Dalprà, L De Carli
Strabismus|February 15, 2011
Brown's syndrome associated with Smith-Magenis syndrome: Case reportR Salati, G Marini, A Degiuli, et al.
Annales De Genetique|January 1, 1996
Further delineation of 7p trisomy. Case report and review of literatureR Pallotta, L Dalprà, P Fusilli, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1985
[Spondylocostal dysostosis]G Bonora, D Baronciani, G Gargantini, et al.
Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia|September 1, 1988
[Dominant epidermolysis bullosa dystrophica of Cockayne-Touraine. Presentation of a familial case and cytogenetic investigation]P Amerio, R Pallotta, D Di Donato, et al.
Minerva Pediatrica|February 28, 1986
[Partial trisomy 9q: comparison of the syndrome in 2 sisters]G P Bianchi, P Cantone, L Dalprà, et al.
Annales De Genetique|January 1, 1993
Prenatal diagnosis of an extranumerary i(22p) with normal phenotypeL Doneda, L Dalprà, M G Tibiletti, et al.
Journal of Medical Genetics|September 19, 2000
Monosomy and trisomy 1q44-qter in two sisters originating from a half cryptic 1q;15p translocationN Villa, E Sala, D Colombo, et al.
Pageof 7