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 (91-100 of 222) with videos related to

Pageof 23
Sort By:
European Journal of Medical Genetics|December 5, 2006
A novel interstitial deletion in Xq25, identified by array-CGH in a patient with Lowe syndromeMaria Addis, Cristiana Meloni, Rita Congiu, et al.
European Journal of Medical Genetics|January 30, 2008
Concurrent transposition of distal 6p and 20q to the 22q telomere: a recurrent benign chromosomal variantMaria Clara Bonaglia, Roberto Giorda, Silvana Beri, et al.
Molecular Cancer|August 1, 2009
The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24.13;q11.21) in a young girl with dysgerminomaStefania Gimelli, Silvana Beri, Harry A Drabkin, et al.
Human Genetics|June 2, 2009
Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhoodFrancesca Novara, Silvana Beri, Maria Ester Bernardo, et al.
Blood Cells, Molecules & Diseases|April 5, 2017
Whole exome sequencing in the differential diagnosis of Diamond-Blackfan anemia: Clinical and molecular study of three patients with novel RPL5 and mosaic RPS19 mutationsEdoardo Errichiello, Annalisa Vetro, Tommaso Mina, et al.
Human Pathology|February 22, 2011
CD5(-) diffuse large B-cell lymphoma with peculiar cyclin D1+ phenotype. Pathologic and molecular characterization of a single caseMarco Lucioni, Francesca Novara, Roberta Riboni, et al.
Neuro-Oncology|October 17, 2008
Presence of 1q gain and absence of 7p gain are new predictors of local or metastatic relapse in localized resectable neuroblastomaAnnalisa Pezzolo, Elena Rossi, Stefania Gimelli, et al.
Journal of Cellular Biochemistry|March 15, 2011
Cell-cycle phases and genetic profile of bone marrow-derived mesenchymal stromal cells expanded in vitro from healthy donorsValentina Achille, Melissa Mantelli, Giulia Arrigo, et al.
Human Genetics|September 1, 2005
Direct duplication 12p11.21-p13.31 mediated by segmental duplications: a new recurrent rearrangement?Manuela De Gregori, Tiziano Pramparo, Luigi Memo, et al.
Human Mutation|November 3, 2016
Clinical and Molecular Characteristics of SLC16A2 (MCT8) Mutations in Three Families with the Allan-Herndon-Dudley SyndromeFrancesca Novara, Stefan Groeneweg, Elena Freri, et al.
Pageof 23

Showing results (91-100 of 222) with videos related to

Sort By:
Pageof 23
European Journal of Medical Genetics|December 5, 2006
A novel interstitial deletion in Xq25, identified by array-CGH in a patient with Lowe syndromeMaria Addis, Cristiana Meloni, Rita Congiu, et al.
European Journal of Medical Genetics|January 30, 2008
Concurrent transposition of distal 6p and 20q to the 22q telomere: a recurrent benign chromosomal variantMaria Clara Bonaglia, Roberto Giorda, Silvana Beri, et al.
Molecular Cancer|August 1, 2009
The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24.13;q11.21) in a young girl with dysgerminomaStefania Gimelli, Silvana Beri, Harry A Drabkin, et al.
Human Genetics|June 2, 2009
Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhoodFrancesca Novara, Silvana Beri, Maria Ester Bernardo, et al.
Blood Cells, Molecules & Diseases|April 5, 2017
Whole exome sequencing in the differential diagnosis of Diamond-Blackfan anemia: Clinical and molecular study of three patients with novel RPL5 and mosaic RPS19 mutationsEdoardo Errichiello, Annalisa Vetro, Tommaso Mina, et al.
Human Pathology|February 22, 2011
CD5(-) diffuse large B-cell lymphoma with peculiar cyclin D1+ phenotype. Pathologic and molecular characterization of a single caseMarco Lucioni, Francesca Novara, Roberta Riboni, et al.
Neuro-Oncology|October 17, 2008
Presence of 1q gain and absence of 7p gain are new predictors of local or metastatic relapse in localized resectable neuroblastomaAnnalisa Pezzolo, Elena Rossi, Stefania Gimelli, et al.
Journal of Cellular Biochemistry|March 15, 2011
Cell-cycle phases and genetic profile of bone marrow-derived mesenchymal stromal cells expanded in vitro from healthy donorsValentina Achille, Melissa Mantelli, Giulia Arrigo, et al.
Human Genetics|September 1, 2005
Direct duplication 12p11.21-p13.31 mediated by segmental duplications: a new recurrent rearrangement?Manuela De Gregori, Tiziano Pramparo, Luigi Memo, et al.
Human Mutation|November 3, 2016
Clinical and Molecular Characteristics of SLC16A2 (MCT8) Mutations in Three Families with the Allan-Herndon-Dudley SyndromeFrancesca Novara, Stefan Groeneweg, Elena Freri, et al.
Pageof 23