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Laura Bernardini

Showing results (81-90 of 157) with videos related to

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Pediatric Pulmonology|April 4, 2025
Genotype-Phenotype Correlation in a Group of Italian Patients With Primary Ciliary DyskinesiaLaura Petrarca, Valentina Guida, Raffaella Nenna, et al.
Genes|December 23, 2022
Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center StudyCarolina Putotto, Federica Pulvirenti, Flaminia Pugnaloni, et al.
Journal of Assisted Reproduction and Genetics|January 27, 2025
Prenatal diagnosis following preimplantation genetic testing (PGT): recommendations of the Italian Society of Human Genetics (SIGU)Francesca Romana Grati, Antonio Capalbo, Ilaria Gabbiato, et al.
American Journal of Medical Genetics. Part A|May 13, 2006
Nablus mask-like facial syndrome is caused by a microdeletion of 8q detected by array-based comparative genomic hybridizationJoseph T C Shieh, Swaroop Aradhya, Antonio Novelli, et al.
Stem Cell Research|June 16, 2019
Production and characterization of human induced pluripotent stem cells (iPSC) CSSi007-A (4383) from Joubert SyndromeFilomena Altieri, Angela D'Anzi, Francesco Martello, et al.
Stem Cell Research|January 18, 2018
Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington DiseaseJessica Rosati, Eris Bidollari, Giovannina Rotundo, et al.
Gene|February 14, 2012
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancerChiara Palka Bayard de Volo, Melissa Alfonsi, Valentina Gatta, et al.
Clinical Case Reports|January 28, 2021
Autism and severe clinical phenotype in a patient with 8p21.2p11.21 deletion: Case report and literature reviewAurora Arghir, Sorina Mihaela Papuc, Andreea-Cristina Tutulan-Cunita, et al.
Stem Cell Research|February 28, 2018
Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stageEris Bidollari, Giovannina Rotundo, Daniela Ferrari, et al.
Stem Cell Research|April 29, 2018
Generation of the induced pluripotent stem cell line CSSi006-A (3681) from a patient affected by advanced-stage Juvenile Onset Huntington's DiseaseGiovannina Rotundo, Eris Bidollari, Daniela Ferrari, et al.
Pageof 16

Showing results (81-90 of 157) with videos related to

Sort By:
Pageof 16
Pediatric Pulmonology|April 4, 2025
Genotype-Phenotype Correlation in a Group of Italian Patients With Primary Ciliary DyskinesiaLaura Petrarca, Valentina Guida, Raffaella Nenna, et al.
Genes|December 23, 2022
Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center StudyCarolina Putotto, Federica Pulvirenti, Flaminia Pugnaloni, et al.
Journal of Assisted Reproduction and Genetics|January 27, 2025
Prenatal diagnosis following preimplantation genetic testing (PGT): recommendations of the Italian Society of Human Genetics (SIGU)Francesca Romana Grati, Antonio Capalbo, Ilaria Gabbiato, et al.
American Journal of Medical Genetics. Part A|May 13, 2006
Nablus mask-like facial syndrome is caused by a microdeletion of 8q detected by array-based comparative genomic hybridizationJoseph T C Shieh, Swaroop Aradhya, Antonio Novelli, et al.
Stem Cell Research|June 16, 2019
Production and characterization of human induced pluripotent stem cells (iPSC) CSSi007-A (4383) from Joubert SyndromeFilomena Altieri, Angela D'Anzi, Francesco Martello, et al.
Stem Cell Research|January 18, 2018
Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington DiseaseJessica Rosati, Eris Bidollari, Giovannina Rotundo, et al.
Gene|February 14, 2012
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancerChiara Palka Bayard de Volo, Melissa Alfonsi, Valentina Gatta, et al.
Clinical Case Reports|January 28, 2021
Autism and severe clinical phenotype in a patient with 8p21.2p11.21 deletion: Case report and literature reviewAurora Arghir, Sorina Mihaela Papuc, Andreea-Cristina Tutulan-Cunita, et al.
Stem Cell Research|February 28, 2018
Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stageEris Bidollari, Giovannina Rotundo, Daniela Ferrari, et al.
Stem Cell Research|April 29, 2018
Generation of the induced pluripotent stem cell line CSSi006-A (3681) from a patient affected by advanced-stage Juvenile Onset Huntington's DiseaseGiovannina Rotundo, Eris Bidollari, Daniela Ferrari, et al.
Pageof 16