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Roberta Santos Guilherme

Showing results (1-10 of 12) with videos related to

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Molecular Cytogenetics|March 15, 2012
Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogeneticsElisabeth Klein, Marina Manvelyan, Isabella Simonyan, et al.
Journal of Applied Genetics|August 29, 2015
Position effect modifying gene expression in a patient with ring chromosome 14Roberta Santos Guilherme, Mariana Moysés-Oliveira, Anelisa Gollo Dantas, et al.
Molecular Syndromology|June 14, 2019
Deletion of Chromosome 13 due to Different Rearrangements and Impact on PhenotypeFernanda T Bellucco, Hélio Rodrigues de Oliveira-Júnior, Roberta Santos Guilherme, et al.
Journal of Applied Genetics|December 19, 2012
Ring chromosome 10: report on two patients and review of the literatureRoberta Santos Guilherme, Chong Ae Kim, Luis Garcia Alonso, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 19, 2012
Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?Roberta Santos Guilherme, Elisabeth Klein, Claudia Venner, et al.
Molecular Cytogenetics|May 14, 2015
Terminal 18q deletions are stabilized by neotelomeresRoberta Santos Guilherme, Karen E Hermetz, Patrícia Teixeira Varela, et al.
Journal of Applied Genetics|May 1, 2012
How to narrow down chromosomal breakpoints in small and large derivative chromosomes--a new probe setAhmed B Hamid, Katharina Kreskowski, Anja Weise, et al.
American Journal of Medical Genetics. Part A|June 6, 2014
Cytogenomic delineation and clinical follow-up of two siblings with an 8.5 Mb 6q24.2-q25.2 deletion inherited from a paternal insertionVera Ayres Meloni, Roberta Santos Guilherme, Mariana Moyses Oliveira, et al.
BMC Medical Genetics|December 21, 2014
Duplication 9p and their implication to phenotypeRoberta Santos Guilherme, Vera Ayres Meloni, Ana Beatriz Alvarez Perez, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 21, 2015
X-linked intellectual disability related genes disrupted by balanced X-autosome translocationsMariana Moysés-Oliveira, Roberta Santos Guilherme, Vera Ayres Meloni, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Molecular Cytogenetics|March 15, 2012
Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogeneticsElisabeth Klein, Marina Manvelyan, Isabella Simonyan, et al.
Journal of Applied Genetics|August 29, 2015
Position effect modifying gene expression in a patient with ring chromosome 14Roberta Santos Guilherme, Mariana Moysés-Oliveira, Anelisa Gollo Dantas, et al.
Molecular Syndromology|June 14, 2019
Deletion of Chromosome 13 due to Different Rearrangements and Impact on PhenotypeFernanda T Bellucco, Hélio Rodrigues de Oliveira-Júnior, Roberta Santos Guilherme, et al.
Journal of Applied Genetics|December 19, 2012
Ring chromosome 10: report on two patients and review of the literatureRoberta Santos Guilherme, Chong Ae Kim, Luis Garcia Alonso, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 19, 2012
Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?Roberta Santos Guilherme, Elisabeth Klein, Claudia Venner, et al.
Molecular Cytogenetics|May 14, 2015
Terminal 18q deletions are stabilized by neotelomeresRoberta Santos Guilherme, Karen E Hermetz, Patrícia Teixeira Varela, et al.
Journal of Applied Genetics|May 1, 2012
How to narrow down chromosomal breakpoints in small and large derivative chromosomes--a new probe setAhmed B Hamid, Katharina Kreskowski, Anja Weise, et al.
American Journal of Medical Genetics. Part A|June 6, 2014
Cytogenomic delineation and clinical follow-up of two siblings with an 8.5 Mb 6q24.2-q25.2 deletion inherited from a paternal insertionVera Ayres Meloni, Roberta Santos Guilherme, Mariana Moyses Oliveira, et al.
BMC Medical Genetics|December 21, 2014
Duplication 9p and their implication to phenotypeRoberta Santos Guilherme, Vera Ayres Meloni, Ana Beatriz Alvarez Perez, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 21, 2015
X-linked intellectual disability related genes disrupted by balanced X-autosome translocationsMariana Moysés-Oliveira, Roberta Santos Guilherme, Vera Ayres Meloni, et al.
Pageof 2