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 (11-20 of 77) with videos related to

Pageof 8
Sort By:
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 24, 2018
Nablus syndrome: Easy to diagnose yet difficult to solveJudith Allanson, Amanda Smith, Francesca Forzano, et al.
Geriatrics & Gerontology International|December 21, 2010
Osteoporosis in an elderly man as interplay of multiple diseasesLuca Foppiani, Alberto Cella, Paola Carrara, et al.
Clinical Dysmorphology|December 24, 2011
A patient with a skull defect, dysmorphic features, hypopituitarism, and abnormal cortical developmentPatrizia Accorsi, Lucio Giordano, Vera Uliana, et al.
European Journal of Human Genetics : EJHG|January 20, 2019
Reply to Bombard and MightonDaniele Carrieri, Heidi C Howard, Angus J Clarke, et al.
Molecular and Cellular Probes|October 20, 2009
The -413C > G substitution in the promoter of the FMR1 gene is not associated with the fragile X syndrome phenotypeMarina Grasso, Massimiliano Cecconi, Stefania Boni, et al.
Pediatric Neurology|February 4, 2014
Setleis syndrome: genetic and clinical findings in a new case with epilepsyLucio Giordano, Robert J Desnick, Anna Molinaro, et al.
The Journal of Molecular Diagnostics : JMD|April 12, 2008
A single nucleotide variant in the FMR1 CGG repeat results in a "Pseudodeletion" and is not associated with the fragile X syndrome phenotypeMassimiliano Cecconi, Francesca Forzano, Rosanna Rinaldi, et al.
American Journal of Medical Genetics. Part A|November 14, 2008
Recurrence of Mowat-Wilson syndrome in siblings with a novel mutation in the ZEB2 geneMassimiliano Cecconi, Francesca Forzano, Livia Garavelli, et al.
European Journal of Human Genetics : EJHG|March 11, 2010
Italian appeal court: a genetic predisposition to commit murder?Francesca Forzano, Pascal Borry, Anne Cambon-Thomsen, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Growth hormone, gender and face shape in Prader-Willi syndromeMauren Abreu de Souza, Catherine McAllister, Michael Suttie, et al.
Pageof 8

Showing results (11-20 of 77) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 24, 2018
Nablus syndrome: Easy to diagnose yet difficult to solveJudith Allanson, Amanda Smith, Francesca Forzano, et al.
Geriatrics & Gerontology International|December 21, 2010
Osteoporosis in an elderly man as interplay of multiple diseasesLuca Foppiani, Alberto Cella, Paola Carrara, et al.
Clinical Dysmorphology|December 24, 2011
A patient with a skull defect, dysmorphic features, hypopituitarism, and abnormal cortical developmentPatrizia Accorsi, Lucio Giordano, Vera Uliana, et al.
European Journal of Human Genetics : EJHG|January 20, 2019
Reply to Bombard and MightonDaniele Carrieri, Heidi C Howard, Angus J Clarke, et al.
Molecular and Cellular Probes|October 20, 2009
The -413C > G substitution in the promoter of the FMR1 gene is not associated with the fragile X syndrome phenotypeMarina Grasso, Massimiliano Cecconi, Stefania Boni, et al.
Pediatric Neurology|February 4, 2014
Setleis syndrome: genetic and clinical findings in a new case with epilepsyLucio Giordano, Robert J Desnick, Anna Molinaro, et al.
The Journal of Molecular Diagnostics : JMD|April 12, 2008
A single nucleotide variant in the FMR1 CGG repeat results in a "Pseudodeletion" and is not associated with the fragile X syndrome phenotypeMassimiliano Cecconi, Francesca Forzano, Rosanna Rinaldi, et al.
American Journal of Medical Genetics. Part A|November 14, 2008
Recurrence of Mowat-Wilson syndrome in siblings with a novel mutation in the ZEB2 geneMassimiliano Cecconi, Francesca Forzano, Livia Garavelli, et al.
European Journal of Human Genetics : EJHG|March 11, 2010
Italian appeal court: a genetic predisposition to commit murder?Francesca Forzano, Pascal Borry, Anne Cambon-Thomsen, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Growth hormone, gender and face shape in Prader-Willi syndromeMauren Abreu de Souza, Catherine McAllister, Michael Suttie, et al.
Pageof 8