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 Lerone

Showing results (31-40 of 70) with videos related to

Pageof 7
Sort By:
Pediatric Surgery International|November 5, 2002
Diagnostic and therapeutic approach to multiple endocrine neoplasia type 2B in pediatric patientsM Torre, G Martucciello, I Ceccherini, et al.
Journal of Medical Genetics|February 7, 2001
Molecular characterisation of a supernumerary ring chromosome in a patient with VATER associationR Cinti, M Priolo, M Lerone, et al.
Clinical Genetics|September 1, 1992
Autosomal recessive microcephaly with early onset seizures and spasticityM Silengo, M Lerone, M Martinelli, et al.
Minerva Medica|March 24, 1981
[Screening of microcythemias in the school population of Latium]E Silvestroni, I Bianco, B Graziani, et al.
Journal of Pediatric Surgery|January 31, 2002
Associated anomalies in intestinal neuronal dysplasiaG Martucciello, M Torre, A Pini Prato, et al.
Minerva Pediatrica|October 1, 1995
[Cardiofacial syndrome. A case report]M Bado, G Morreale, M Pelegrini, et al.
Clinical Dysmorphology|May 11, 2002
Auriculo-condylar syndrome or new syndrome?M T Divizia, A Cordone, M Bado, et al.
Journal of Pediatric Surgery|September 11, 2004
Currarino syndrome: proposal of a diagnostic and therapeutic protocolG Martucciello, M Torre, E Belloni, et al.
Journal of Medical Genetics|June 1, 1980
Screening of thalassaemia carriers in intermediate school of Latium: results of four years' workE Silvestroni, I Bianco, B Graziani, et al.
Clinical Genetics|August 17, 2000
Pfeiffer syndrome type 2 associated with a single amino acid deletion in the FGFR2 geneM Priolo, M Lerone, M Baffico, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
Pediatric Surgery International|November 5, 2002
Diagnostic and therapeutic approach to multiple endocrine neoplasia type 2B in pediatric patientsM Torre, G Martucciello, I Ceccherini, et al.
Journal of Medical Genetics|February 7, 2001
Molecular characterisation of a supernumerary ring chromosome in a patient with VATER associationR Cinti, M Priolo, M Lerone, et al.
Clinical Genetics|September 1, 1992
Autosomal recessive microcephaly with early onset seizures and spasticityM Silengo, M Lerone, M Martinelli, et al.
Minerva Medica|March 24, 1981
[Screening of microcythemias in the school population of Latium]E Silvestroni, I Bianco, B Graziani, et al.
Journal of Pediatric Surgery|January 31, 2002
Associated anomalies in intestinal neuronal dysplasiaG Martucciello, M Torre, A Pini Prato, et al.
Minerva Pediatrica|October 1, 1995
[Cardiofacial syndrome. A case report]M Bado, G Morreale, M Pelegrini, et al.
Clinical Dysmorphology|May 11, 2002
Auriculo-condylar syndrome or new syndrome?M T Divizia, A Cordone, M Bado, et al.
Journal of Pediatric Surgery|September 11, 2004
Currarino syndrome: proposal of a diagnostic and therapeutic protocolG Martucciello, M Torre, E Belloni, et al.
Journal of Medical Genetics|June 1, 1980
Screening of thalassaemia carriers in intermediate school of Latium: results of four years' workE Silvestroni, I Bianco, B Graziani, et al.
Clinical Genetics|August 17, 2000
Pfeiffer syndrome type 2 associated with a single amino acid deletion in the FGFR2 geneM Priolo, M Lerone, M Baffico, et al.
Pageof 7