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 (41-50 of 130) with videos related to

Pageof 13
Sort By:
American Journal of Medical Genetics|December 31, 1997
Progeroid syndrome with characteristic facial appearance and hand anomalies in father and sonA Giannotti, M C Digilio, R Mingarelli, et al.
Clinical Genetics|September 1, 1995
Joint dislocation and cerebral anomalies are consistently associated with oral-facial-digital syndrome type IVM C Digilio, A Giannotti, G Pagnotta, et al.
Clinical Dysmorphology|October 1, 1995
Sporadic trichodental dysplasia with microcephaly and mental retardationA Giannotti, M C Digilio, G Albertini, et al.
Human Mutation|February 22, 2002
Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangismM Mangino, E Flex, M C Digilio, et al.
Journal of Medical Genetics|March 2, 1999
Microdeletion 22q11 and oesophageal atresiaM C Digilio, B Marino, P Bagolan, et al.
Giornale Italiano Di Cardiologia|February 1, 1994
[Genetics of congenital heart diseases]B Dallapiccola, R Mingarelli, M C Digilio, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11B Marino, M C Digilio, A Toscano, et al.
American Journal of Medical Genetics|March 1, 1992
New case of Bartsocas-Papas syndrome surviving at 20 monthsA Giannotti, M C Digilio, L Standoli, et al.
The Journal of Pediatrics|December 10, 1999
Congenital heart diseases in children with Noonan syndrome: An expanded cardiac spectrum with high prevalence of atrioventricular canalB Marino, M C Digilio, A Toscano, et al.
American Journal of Medical Genetics|February 7, 1998
Intrafamilial variability of Pfeiffer-type cardiocranial syndromeM C Digilio, B Marino, U Borzaga, et al.
Pageof 13

Showing results (41-50 of 130) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics|December 31, 1997
Progeroid syndrome with characteristic facial appearance and hand anomalies in father and sonA Giannotti, M C Digilio, R Mingarelli, et al.
Clinical Genetics|September 1, 1995
Joint dislocation and cerebral anomalies are consistently associated with oral-facial-digital syndrome type IVM C Digilio, A Giannotti, G Pagnotta, et al.
Clinical Dysmorphology|October 1, 1995
Sporadic trichodental dysplasia with microcephaly and mental retardationA Giannotti, M C Digilio, G Albertini, et al.
Human Mutation|February 22, 2002
Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangismM Mangino, E Flex, M C Digilio, et al.
Journal of Medical Genetics|March 2, 1999
Microdeletion 22q11 and oesophageal atresiaM C Digilio, B Marino, P Bagolan, et al.
Giornale Italiano Di Cardiologia|February 1, 1994
[Genetics of congenital heart diseases]B Dallapiccola, R Mingarelli, M C Digilio, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11B Marino, M C Digilio, A Toscano, et al.
American Journal of Medical Genetics|March 1, 1992
New case of Bartsocas-Papas syndrome surviving at 20 monthsA Giannotti, M C Digilio, L Standoli, et al.
The Journal of Pediatrics|December 10, 1999
Congenital heart diseases in children with Noonan syndrome: An expanded cardiac spectrum with high prevalence of atrioventricular canalB Marino, M C Digilio, A Toscano, et al.
American Journal of Medical Genetics|February 7, 1998
Intrafamilial variability of Pfeiffer-type cardiocranial syndromeM C Digilio, B Marino, U Borzaga, et al.
Pageof 13