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

O Zuffardi

Showing results (151-160 of 159) with videos related to

Pageof 16
Sort By:
You have reached the last page of results.This site can display upto 159 results.
Leukemia|May 21, 2010
Bone osteoblastic and mesenchymal stromal cells lack primarily tumoral features in multiple myeloma patientsN Giuliani, G Lisignoli, F Novara, et al.
Circulation|July 25, 2000
Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defectsS Giglio, S L Graw, G Gimelli, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 21, 2012
Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011A Novelli, F R Grati, L Ballarati, et al.
Journal of Medical Genetics|June 27, 2001
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformationsE Rossi, F Piccini, M Zollino, et al.
Leukemia|March 13, 2014
Functional and genetic aberrations of in vitro-cultured marrow-derived mesenchymal stromal cells of patients with classical Philadelphia-negative myeloproliferative neoplasmsM A Avanzini, M E Bernardo, F Novara, et al.
Molecular Syndromology|December 6, 2011
Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 MicroduplicationsJ Wincent, D L Bruno, B W M van Bon, et al.
Journal of Medical Genetics|January 8, 2008
Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesisB W M van Bon, D A Koolen, R Borgatti, et al.
Journal of Medical Genetics|September 4, 2007
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patientsM De Gregori, R Ciccone, P Magini, et al.
Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.
Pageof 16

Showing results (151-160 of 159) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 159 results.
Leukemia|May 21, 2010
Bone osteoblastic and mesenchymal stromal cells lack primarily tumoral features in multiple myeloma patientsN Giuliani, G Lisignoli, F Novara, et al.
Circulation|July 25, 2000
Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defectsS Giglio, S L Graw, G Gimelli, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 21, 2012
Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011A Novelli, F R Grati, L Ballarati, et al.
Journal of Medical Genetics|June 27, 2001
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformationsE Rossi, F Piccini, M Zollino, et al.
Leukemia|March 13, 2014
Functional and genetic aberrations of in vitro-cultured marrow-derived mesenchymal stromal cells of patients with classical Philadelphia-negative myeloproliferative neoplasmsM A Avanzini, M E Bernardo, F Novara, et al.
Molecular Syndromology|December 6, 2011
Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 MicroduplicationsJ Wincent, D L Bruno, B W M van Bon, et al.
Journal of Medical Genetics|January 8, 2008
Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesisB W M van Bon, D A Koolen, R Borgatti, et al.
Journal of Medical Genetics|September 4, 2007
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patientsM De Gregori, R Ciccone, P Magini, et al.
Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.
Pageof 16