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

M C Digilio

Showing results (81-90 of 130) with videos related to

Pageof 13
Sort By:
American Journal of Otolaryngology|December 15, 2000
Nasal cartilage aplasia in a family with facioaudiosymphalangism syndromeM G Obregon, M C Digilio, R Mingarelli, et al.
Clinical Genetics|April 19, 2003
Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomaliesM C Digilio, A Angioni, M De Santis, et al.
The American Journal of Cardiology|September 25, 1999
Deletion 22q11 in patients with interrupted aortic archB Marino, M C Digilio, M Persiani, et al.
Clinical Genetics|February 11, 2018
Intrafamiliar clinical variability of circumferential skin creases Kunze type caused by a novel heterozygous mutation of N-terminal TUBB geneM L Dentici, A Terracciano, E Bellacchio, et al.
Clinical Genetics|June 18, 2004
High frequency of subtelomeric rearrangements in a cohort of 92 patients with severe mental retardation and dysmorphismA Novelli, C Ceccarini, L Bernardini, et al.
Molecular and Cellular Probes|August 11, 1999
Diagnosis of DiGeorge and Williams syndromes using FISH analysis of peripheral blood smearsA Novelli, M Sabani, A Caiola, et al.
Human Genetics|May 1, 1995
22q11 deletions in isolated and syndromic patients with tetralogy of FallotF Amati, A Mari, M C Digilio, et al.
Journal of Craniofacial Genetics and Developmental Biology|April 1, 1996
The search for hemizygosity at 22qll in patients with isolated cleft palateR Mingarelli, M C Digilio, A Mari, et al.
Journal of Medical Genetics|October 1, 1992
Familial postaxial acrofacial dysostosis syndromeA Giannotti, M C Digilio, Q Virgili, et al.
Journal of Medical Genetics|March 1, 1994
Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum developmentM C Digilio, A Giannotti, G Floridia, et al.
Pageof 13

Showing results (81-90 of 130) with videos related to

Sort By:
Pageof 13
American Journal of Otolaryngology|December 15, 2000
Nasal cartilage aplasia in a family with facioaudiosymphalangism syndromeM G Obregon, M C Digilio, R Mingarelli, et al.
Clinical Genetics|April 19, 2003
Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomaliesM C Digilio, A Angioni, M De Santis, et al.
The American Journal of Cardiology|September 25, 1999
Deletion 22q11 in patients with interrupted aortic archB Marino, M C Digilio, M Persiani, et al.
Clinical Genetics|February 11, 2018
Intrafamiliar clinical variability of circumferential skin creases Kunze type caused by a novel heterozygous mutation of N-terminal TUBB geneM L Dentici, A Terracciano, E Bellacchio, et al.
Clinical Genetics|June 18, 2004
High frequency of subtelomeric rearrangements in a cohort of 92 patients with severe mental retardation and dysmorphismA Novelli, C Ceccarini, L Bernardini, et al.
Molecular and Cellular Probes|August 11, 1999
Diagnosis of DiGeorge and Williams syndromes using FISH analysis of peripheral blood smearsA Novelli, M Sabani, A Caiola, et al.
Human Genetics|May 1, 1995
22q11 deletions in isolated and syndromic patients with tetralogy of FallotF Amati, A Mari, M C Digilio, et al.
Journal of Craniofacial Genetics and Developmental Biology|April 1, 1996
The search for hemizygosity at 22qll in patients with isolated cleft palateR Mingarelli, M C Digilio, A Mari, et al.
Journal of Medical Genetics|October 1, 1992
Familial postaxial acrofacial dysostosis syndromeA Giannotti, M C Digilio, Q Virgili, et al.
Journal of Medical Genetics|March 1, 1994
Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum developmentM C Digilio, A Giannotti, G Floridia, et al.
Pageof 13