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Francesca Forzano

Showing results (1-10 of 77) with videos related to

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European Journal of Human Genetics : EJHG|February 20, 2021
Correction: ESHG warns against misuses of genetic tests and biobanks for discrimination purposesFrancesca Forzano, Maurizio Genuardi, Yves Moreau, et al.
Frontiers in Neurology|August 9, 2021
Editorial: Overlapping Phenotypes and Genetic Heterogeneity of Rare Neurodevelopmental DisordersFrancesca Cogliati, Francesca Forzano, Silvia Russo
European Journal of Human Genetics : EJHG|January 18, 2021
ESHG warns against misuses of genetic tests and biobanks for discrimination purposesFrancesca Forzano, Maurizio Genuardi, Yves Moreau, et al.
American Journal of Medical Genetics. Part A|April 6, 2005
Midline raphé, sternal cleft, and other midline abnormalities: a new dominant syndrome?Francesca Forzano, Piers E F Daubeney, Susan M White
American Journal of Obstetrics and Gynecology|May 2, 2024
Prediction of venous thromboembolism in average-risk, young candidates for oral contraceptive use: to genotype, or not to genotype, that is the questionPaolo Vercellini, Andrea Artoni, Maria Abbattista, et al.
Ebiomedicine|November 9, 2023
A genomic perspective on climate changeFrancesca Forzano, Chantal Babb de Villiers, Martin Farley, et al.
Prenatal Diagnosis|September 19, 2006
Fetal aortic root dilation: a prenatal feature of the Loeys-Dietz syndromeValeria Viassolo, Mario Lituania, Maurizio Marasini, et al.
Forensic Science International. Genetics|July 22, 2018
A response to the forensic genetics policy initiative's report "Establishing Best Practice for Forensic DNA Databases"Gabrielle Samuel, Heidi Carmen Howard, Martina Cornel, et al.
Human Genetics|October 29, 2018
Lowry-Wood syndrome: further evidence of association with RNU4ATAC, and correlation between genotype and phenotypeIvan Shelihan, Sophie Ehresmann, Cinzia Magnani, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 17, 2010
The refinement of the critical region for the 2q31.2q32.3 deletion syndrome indicates candidate genes for mental retardation and speech impairmentAlessandro Cocchella, Michela Malacarne, Francesca Forzano, et al.
Pageof 8

Showing results (1-10 of 77) with videos related to

Sort By:
Pageof 8
European Journal of Human Genetics : EJHG|February 20, 2021
Correction: ESHG warns against misuses of genetic tests and biobanks for discrimination purposesFrancesca Forzano, Maurizio Genuardi, Yves Moreau, et al.
Frontiers in Neurology|August 9, 2021
Editorial: Overlapping Phenotypes and Genetic Heterogeneity of Rare Neurodevelopmental DisordersFrancesca Cogliati, Francesca Forzano, Silvia Russo
European Journal of Human Genetics : EJHG|January 18, 2021
ESHG warns against misuses of genetic tests and biobanks for discrimination purposesFrancesca Forzano, Maurizio Genuardi, Yves Moreau, et al.
American Journal of Medical Genetics. Part A|April 6, 2005
Midline raphé, sternal cleft, and other midline abnormalities: a new dominant syndrome?Francesca Forzano, Piers E F Daubeney, Susan M White
American Journal of Obstetrics and Gynecology|May 2, 2024
Prediction of venous thromboembolism in average-risk, young candidates for oral contraceptive use: to genotype, or not to genotype, that is the questionPaolo Vercellini, Andrea Artoni, Maria Abbattista, et al.
Ebiomedicine|November 9, 2023
A genomic perspective on climate changeFrancesca Forzano, Chantal Babb de Villiers, Martin Farley, et al.
Prenatal Diagnosis|September 19, 2006
Fetal aortic root dilation: a prenatal feature of the Loeys-Dietz syndromeValeria Viassolo, Mario Lituania, Maurizio Marasini, et al.
Forensic Science International. Genetics|July 22, 2018
A response to the forensic genetics policy initiative's report "Establishing Best Practice for Forensic DNA Databases"Gabrielle Samuel, Heidi Carmen Howard, Martina Cornel, et al.
Human Genetics|October 29, 2018
Lowry-Wood syndrome: further evidence of association with RNU4ATAC, and correlation between genotype and phenotypeIvan Shelihan, Sophie Ehresmann, Cinzia Magnani, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 17, 2010
The refinement of the critical region for the 2q31.2q32.3 deletion syndrome indicates candidate genes for mental retardation and speech impairmentAlessandro Cocchella, Michela Malacarne, Francesca Forzano, et al.
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