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

Francesca Forzano

Showing results (21-30 of 77) with videos related to

Pageof 8
Sort By:
Prenatal Diagnosis|April 9, 2009
Prenatal diagnosis of Gollop-Wolfgang ComplexFrancesca Forzano, V Viassolo, M Castagnetta, et al.
European Journal of Human Genetics : EJHG|October 10, 2019
ESHG PPPC Comments on postmortem use of genetic data for research purposesFlorence Fellmann, Emmanuelle Rial-Sebbag, Christine Patch, et al.
Frontiers in Genetics|November 20, 2018
FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the <i>FMR1</i> GeneEsperanza Fernández, Elena Gennaro, Filomena Pirozzi, et al.
European Journal of Human Genetics : EJHG|December 2, 2017
One small edit for humans, one giant edit for humankind? Points and questions to consider for a responsible way forward for gene editing in humansHeidi C Howard, Carla G van El, Francesca Forzano, et al.
European Journal of Medical Genetics|April 19, 2012
19q13 microdeletion syndrome: Further refining the critical regionFrancesca Forzano, Flavia Napoli, Vera Uliana, et al.
European Journal of Human Genetics : EJHG|December 6, 2012
Craniofacial characteristics of fragile X syndrome in mouse and manInge Heulens, Michael Suttie, Andrei Postnov, et al.
Annals of Clinical and Translational Neurology|August 13, 2019
P5CS expression study in a new family with ALDH18A1-associated hereditary spastic paraplegia SPG9Pamela Magini, Clara Marco-Marin, Juan M Escamilla-Honrubia, et al.
Human Reproduction (Oxford, England)|June 14, 2024
An ESHG-ESHRE survey on the current practice of expanded carrier screening in medically assisted reproductionAntonio Capalbo, Guido de Wert, Lidewij Henneman, et al.
Clinical Dysmorphology|September 30, 2017
Contiguous gene deletion of TBX5 and TBX3: report of another caseFrancesca Forzano, Patricia A Foley, Morgan R Keane, et al.
European Journal of Medical Genetics|January 30, 2013
3q26.33-3q27.2 microdeletion: a new microdeletion syndrome?Giorgia Mandrile, Anna Dubois, Jodi D Hoffman, et al.
Pageof 8

Showing results (21-30 of 77) with videos related to

Sort By:
Pageof 8
Prenatal Diagnosis|April 9, 2009
Prenatal diagnosis of Gollop-Wolfgang ComplexFrancesca Forzano, V Viassolo, M Castagnetta, et al.
European Journal of Human Genetics : EJHG|October 10, 2019
ESHG PPPC Comments on postmortem use of genetic data for research purposesFlorence Fellmann, Emmanuelle Rial-Sebbag, Christine Patch, et al.
Frontiers in Genetics|November 20, 2018
FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the <i>FMR1</i> GeneEsperanza Fernández, Elena Gennaro, Filomena Pirozzi, et al.
European Journal of Human Genetics : EJHG|December 2, 2017
One small edit for humans, one giant edit for humankind? Points and questions to consider for a responsible way forward for gene editing in humansHeidi C Howard, Carla G van El, Francesca Forzano, et al.
European Journal of Medical Genetics|April 19, 2012
19q13 microdeletion syndrome: Further refining the critical regionFrancesca Forzano, Flavia Napoli, Vera Uliana, et al.
European Journal of Human Genetics : EJHG|December 6, 2012
Craniofacial characteristics of fragile X syndrome in mouse and manInge Heulens, Michael Suttie, Andrei Postnov, et al.
Annals of Clinical and Translational Neurology|August 13, 2019
P5CS expression study in a new family with ALDH18A1-associated hereditary spastic paraplegia SPG9Pamela Magini, Clara Marco-Marin, Juan M Escamilla-Honrubia, et al.
Human Reproduction (Oxford, England)|June 14, 2024
An ESHG-ESHRE survey on the current practice of expanded carrier screening in medically assisted reproductionAntonio Capalbo, Guido de Wert, Lidewij Henneman, et al.
Clinical Dysmorphology|September 30, 2017
Contiguous gene deletion of TBX5 and TBX3: report of another caseFrancesca Forzano, Patricia A Foley, Morgan R Keane, et al.
European Journal of Medical Genetics|January 30, 2013
3q26.33-3q27.2 microdeletion: a new microdeletion syndrome?Giorgia Mandrile, Anna Dubois, Jodi D Hoffman, et al.
Pageof 8