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Silvia Milani

Showing results (11-20 of 21) with videos related to

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Soft Matter|September 10, 2020
Collective headgroup conformational transition in twisted micellar superstructuresFrancesca Baldelli Bombelli, Debora Berti, Silvia Milani, et al.
Epidemiologia E Prevenzione|May 21, 2008
[Geographical analysis of mortality in a municipality of the Veneto region, where a landfill is located, and the surrounding area. Years 1995-2003]Gianstefano Blengio, Enrica Castellani, Damiano Dalla Costa, et al.
ACS Nano|December 28, 2016
Understanding the Kinetics of Protein-Nanoparticle Corona FormationOriol Vilanova, Judith J Mittag, Philip M Kelly, et al.
European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|October 20, 2012
Comparison of four different particle sizing methods for siRNA polyplex characterizationChristina Troiber, Julia C Kasper, Silvia Milani, et al.
European Journal of Human Genetics : EJHG|January 19, 2006
Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villiFrancesca R Grati, Beatrice Grimi, Giuditia Frascoli, et al.
Prenatal Diagnosis|October 23, 2016
Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indicationsJose Carlos P Ferreira, Francesca R Grati, Komal Bajaj, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
Pure monosomy and pure trisomy of 13q21.2-31.1 consequent to a familial insertional translocation: exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1)Francesca R Grati, Marci M Lesperance, Simona De Toffol, et al.
Molecular and Cellular Probes|July 29, 2008
Prenatal detection by subtelomeric FISH and MLPA of unbalanced meiotic recombinants resulting from parental pericentric inversionsFrancesca R Grati, Sara Chinetti, Roberta Malgara, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Chromosome abnormalities investigated by non-invasive prenatal testing account for approximately 50% of fetal unbalances associated with relevant clinical phenotypesFrancesca Romana Grati, Andrea Barlocco, Beatrice Grimi, et al.
Prenatal Diagnosis|April 23, 2013
QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first-trimester prenatal diagnosesFrancesca R Grati, Francesca Malvestiti, Beatrice Grimi, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Soft Matter|September 10, 2020
Collective headgroup conformational transition in twisted micellar superstructuresFrancesca Baldelli Bombelli, Debora Berti, Silvia Milani, et al.
Epidemiologia E Prevenzione|May 21, 2008
[Geographical analysis of mortality in a municipality of the Veneto region, where a landfill is located, and the surrounding area. Years 1995-2003]Gianstefano Blengio, Enrica Castellani, Damiano Dalla Costa, et al.
ACS Nano|December 28, 2016
Understanding the Kinetics of Protein-Nanoparticle Corona FormationOriol Vilanova, Judith J Mittag, Philip M Kelly, et al.
European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|October 20, 2012
Comparison of four different particle sizing methods for siRNA polyplex characterizationChristina Troiber, Julia C Kasper, Silvia Milani, et al.
European Journal of Human Genetics : EJHG|January 19, 2006
Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villiFrancesca R Grati, Beatrice Grimi, Giuditia Frascoli, et al.
Prenatal Diagnosis|October 23, 2016
Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indicationsJose Carlos P Ferreira, Francesca R Grati, Komal Bajaj, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
Pure monosomy and pure trisomy of 13q21.2-31.1 consequent to a familial insertional translocation: exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1)Francesca R Grati, Marci M Lesperance, Simona De Toffol, et al.
Molecular and Cellular Probes|July 29, 2008
Prenatal detection by subtelomeric FISH and MLPA of unbalanced meiotic recombinants resulting from parental pericentric inversionsFrancesca R Grati, Sara Chinetti, Roberta Malgara, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Chromosome abnormalities investigated by non-invasive prenatal testing account for approximately 50% of fetal unbalances associated with relevant clinical phenotypesFrancesca Romana Grati, Andrea Barlocco, Beatrice Grimi, et al.
Prenatal Diagnosis|April 23, 2013
QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first-trimester prenatal diagnosesFrancesca R Grati, Francesca Malvestiti, Beatrice Grimi, et al.
Pageof 3