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

Roberta S Guilherme

Showing results (1-10 of 7) with videos related to

Pageof 1
Sort By:
Journal of Medical Case Reports|September 11, 2012
Twenty-year cytogenetic and molecular follow-up of a patient with ring chromosome 15: a case reportRoberta S Guilherme, Vera de Fa Meloni, Sylvia S Takeno, et al.
Cytogenetic and Genome Research|February 27, 2016
Atypical 581-kb 22q11.21 Deletion in a Patient with Oculo-Auriculo-Vertebral Spectrum PhenotypeMileny E S Colovati, Silvia Bragagnolo, Roberta S Guilherme, et al.
Cytogenetic and Genome Research|November 15, 2016
Wolf-Hirschhorn Syndrome with Epibulbar Dermoid: An Unusual Association in a Patient with 4p Deletion and Functional Xp DisomySilvia Bragagnolo, Mileny E S Colovati, Roberta S Guilherme, et al.
BMC Medical Genetics|December 23, 2011
Mechanisms of ring chromosome formation, ring instability and clinical consequencesRoberta S Guilherme, Vera F Ayres Meloni, Chong A Kim, et al.
Molecular Cytogenetics|January 21, 2012
Marfan syndrome with a complex chromosomal rearrangement including deletion of the FBN1 geneMileny Es Colovati, Luciana Rj da Silva, Sylvia S Takeno, et al.
The Journal of Pediatrics|July 24, 2013
Single-nucleotide polymorphism array-based characterization of ring chromosome 18Ana Spreiz, Roberta S Guilherme, Claudio Castellan, et al.
Molecular Cytogenetics|November 1, 2013
Complex small supernumerary marker chromosomes - an updateThomas Liehr, Sanja Cirkovic, Tanja Lalic, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Journal of Medical Case Reports|September 11, 2012
Twenty-year cytogenetic and molecular follow-up of a patient with ring chromosome 15: a case reportRoberta S Guilherme, Vera de Fa Meloni, Sylvia S Takeno, et al.
Cytogenetic and Genome Research|February 27, 2016
Atypical 581-kb 22q11.21 Deletion in a Patient with Oculo-Auriculo-Vertebral Spectrum PhenotypeMileny E S Colovati, Silvia Bragagnolo, Roberta S Guilherme, et al.
Cytogenetic and Genome Research|November 15, 2016
Wolf-Hirschhorn Syndrome with Epibulbar Dermoid: An Unusual Association in a Patient with 4p Deletion and Functional Xp DisomySilvia Bragagnolo, Mileny E S Colovati, Roberta S Guilherme, et al.
BMC Medical Genetics|December 23, 2011
Mechanisms of ring chromosome formation, ring instability and clinical consequencesRoberta S Guilherme, Vera F Ayres Meloni, Chong A Kim, et al.
Molecular Cytogenetics|January 21, 2012
Marfan syndrome with a complex chromosomal rearrangement including deletion of the FBN1 geneMileny Es Colovati, Luciana Rj da Silva, Sylvia S Takeno, et al.
The Journal of Pediatrics|July 24, 2013
Single-nucleotide polymorphism array-based characterization of ring chromosome 18Ana Spreiz, Roberta S Guilherme, Claudio Castellan, et al.
Molecular Cytogenetics|November 1, 2013
Complex small supernumerary marker chromosomes - an updateThomas Liehr, Sanja Cirkovic, Tanja Lalic, et al.
Pageof 1