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

Orsetta Zuffardi

Showing results (151-160 of 222) with videos related to

Pageof 23
Sort By:
European Journal of Human Genetics : EJHG|January 15, 2015
Reply to Sajantila and BudowleDavid E Barton, Mireille Claustres, Viktor Kozich, et al.
European Journal of Human Genetics : EJHG|July 24, 2008
Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotypeMaria Clara Bonaglia, Roberto Ciccone, Giorgio Gimelli, et al.
European Journal of Human Genetics : EJHG|July 22, 2010
Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletionsMaria C Bonaglia, Susan Marelli, Francesca Novara, et al.
European Journal of Human Genetics : EJHG|February 16, 2017
MCM5: a new actor in the link between DNA replication and Meier-Gorlin syndromeAnnalisa Vetro, Salvatore Savasta, Annalisa Russo Raucci, et al.
Human Mutation|October 21, 2010
Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tractStefania Gimelli, Gianluca Caridi, Silvana Beri, et al.
Cytotherapy|November 12, 2009
Phenotypical/functional characterization of in vitro-expanded mesenchymal stromal cells from patients with Crohn's diseaseMaria Ester Bernardo, Maria Antonia Avanzini, Rachele Ciccocioppo, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
Search for genomic imbalances in a cohort of 20 patients with oral-facial-digital syndromes negative for mutations and large rearrangements in the OFD1 geneChristel Thauvin-Robinet, Patrick Callier, Brunella Franco, et al.
Hypertension (Dallas, Tex. : 1979)|December 13, 2017
Three Reportedly Unrelated Families With Liddle Syndrome Inherited From a Common AncestorLuca Pagani, Yoan Diekmann, Marco Sazzini, et al.
Human Pathology|August 4, 2009
High-resolution genome-wide array comparative genomic hybridization in splenic marginal zone B-cell lymphomaFrancesca Novara, Luca Arcaini, Michele Merli, et al.
European Journal of Human Genetics : EJHG|August 15, 2013
Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic)Mireille Claustres, Viktor Kožich, Els Dequeker, et al.
Pageof 23

Showing results (151-160 of 222) with videos related to

Sort By:
Pageof 23
European Journal of Human Genetics : EJHG|January 15, 2015
Reply to Sajantila and BudowleDavid E Barton, Mireille Claustres, Viktor Kozich, et al.
European Journal of Human Genetics : EJHG|July 24, 2008
Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotypeMaria Clara Bonaglia, Roberto Ciccone, Giorgio Gimelli, et al.
European Journal of Human Genetics : EJHG|July 22, 2010
Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletionsMaria C Bonaglia, Susan Marelli, Francesca Novara, et al.
European Journal of Human Genetics : EJHG|February 16, 2017
MCM5: a new actor in the link between DNA replication and Meier-Gorlin syndromeAnnalisa Vetro, Salvatore Savasta, Annalisa Russo Raucci, et al.
Human Mutation|October 21, 2010
Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tractStefania Gimelli, Gianluca Caridi, Silvana Beri, et al.
Cytotherapy|November 12, 2009
Phenotypical/functional characterization of in vitro-expanded mesenchymal stromal cells from patients with Crohn's diseaseMaria Ester Bernardo, Maria Antonia Avanzini, Rachele Ciccocioppo, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
Search for genomic imbalances in a cohort of 20 patients with oral-facial-digital syndromes negative for mutations and large rearrangements in the OFD1 geneChristel Thauvin-Robinet, Patrick Callier, Brunella Franco, et al.
Hypertension (Dallas, Tex. : 1979)|December 13, 2017
Three Reportedly Unrelated Families With Liddle Syndrome Inherited From a Common AncestorLuca Pagani, Yoan Diekmann, Marco Sazzini, et al.
Human Pathology|August 4, 2009
High-resolution genome-wide array comparative genomic hybridization in splenic marginal zone B-cell lymphomaFrancesca Novara, Luca Arcaini, Michele Merli, et al.
European Journal of Human Genetics : EJHG|August 15, 2013
Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic)Mireille Claustres, Viktor Kožich, Els Dequeker, et al.
Pageof 23