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

V Cirigliano

Showing results (1-10 of 26) with videos related to

Pageof 3
Sort By:
Journal of Medical Genetics|May 12, 2000
Detection of fetal cells in transcervical samples using X22 markerM Adinolfi, V Cirigliano
Physical Review Letters|November 13, 2003
Isospin violation in epsilon'V Cirigliano, A Pich, G Ecker, et al.
Annals of Human Genetics|July 11, 1998
Assessment of diagnostic quantitative fluorescent multiplex polymerase chain reaction assays performed on single cellsJ Sherlock, V Cirigliano, M Petrou, et al.
Physical Review Letters|December 17, 2004
Neutrinoless double Beta decay and lepton flavor violationV Cirigliano, A Kurylov, M J Ramsey-Musolf, et al.
Annals of Human Genetics|January 25, 2002
Assessment of new markers for the rapid detection of aneuploidies by quantitative fluorescent PCR (QF-PCR)V Cirigliano, P Lewin, S Szpiro-Tapies, et al.
Leukemia & Lymphoma|October 1, 1995
Double isochromosome 8q as single cytogenetic aberration in acute myelo-monocytic leukemiaL Vicari, L Sebastio, V Cirigliano, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 17, 2016
Performance of the neoBona test: a new paired-end massively parallel shotgun sequencing approach for cell-free DNA-based aneuploidy screeningV Cirigliano, E Ordoñez, L Rueda, et al.
Prenatal Diagnosis|December 11, 1999
Rapid detection of chromosomes X and Y aneuploidies by quantitative fluorescent PCRV Cirigliano, J Sherlock, G Conway, et al.
Fetal Diagnosis and Therapy|March 15, 2013
Supernumerary ring chromosome: an etiology for Pallister-Killian syndrome?E Lloveras, A Canellas, V Cirigliano, et al.
Clinical Genetics|February 11, 2000
Transcervical cells and the prenatal diagnosis of haemoglobin (Hb) mutationsV Cirigliano, J Sherlock, M Petrou, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|May 12, 2000
Detection of fetal cells in transcervical samples using X22 markerM Adinolfi, V Cirigliano
Physical Review Letters|November 13, 2003
Isospin violation in epsilon'V Cirigliano, A Pich, G Ecker, et al.
Annals of Human Genetics|July 11, 1998
Assessment of diagnostic quantitative fluorescent multiplex polymerase chain reaction assays performed on single cellsJ Sherlock, V Cirigliano, M Petrou, et al.
Physical Review Letters|December 17, 2004
Neutrinoless double Beta decay and lepton flavor violationV Cirigliano, A Kurylov, M J Ramsey-Musolf, et al.
Annals of Human Genetics|January 25, 2002
Assessment of new markers for the rapid detection of aneuploidies by quantitative fluorescent PCR (QF-PCR)V Cirigliano, P Lewin, S Szpiro-Tapies, et al.
Leukemia & Lymphoma|October 1, 1995
Double isochromosome 8q as single cytogenetic aberration in acute myelo-monocytic leukemiaL Vicari, L Sebastio, V Cirigliano, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 17, 2016
Performance of the neoBona test: a new paired-end massively parallel shotgun sequencing approach for cell-free DNA-based aneuploidy screeningV Cirigliano, E Ordoñez, L Rueda, et al.
Prenatal Diagnosis|December 11, 1999
Rapid detection of chromosomes X and Y aneuploidies by quantitative fluorescent PCRV Cirigliano, J Sherlock, G Conway, et al.
Fetal Diagnosis and Therapy|March 15, 2013
Supernumerary ring chromosome: an etiology for Pallister-Killian syndrome?E Lloveras, A Canellas, V Cirigliano, et al.
Clinical Genetics|February 11, 2000
Transcervical cells and the prenatal diagnosis of haemoglobin (Hb) mutationsV Cirigliano, J Sherlock, M Petrou, et al.
Pageof 3