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Maria Isabel Melaragno

Showing results (71-80 of 86) with videos related to

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Genetics Research|April 8, 2024
Variants in Candidate Genes for Phenotype Heterogeneity in Patients with the 22q11.2 Deletion SyndromeNatalia Nunes, Beatriz Carvalho Nunes, Malú Zamariolli, et al.
Journal of Intellectual Disabilities : JOID|September 30, 2009
Evaluation of clinical checklists for fragile X syndrome screening in Brazilian intellectually disabled males: proposal for a new screening toolDenise M Christofolini, Eduardo M Abbud, Monica V N Lipay, et al.
World Journal of Gastroenterology|December 7, 2016
Identification of <i>IL11RA</i> and <i>MELK</i> amplification in gastric cancer by comprehensive genomic profiling of gastric cancer cell linesDanielle Queiroz Calcagno, Sylvia Santomi Takeno, Carolina Oliveira Gigek, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
A rare case of trisomy 15pter-q21.2 due to a de novo marker chromosomeAde Nubia Xavier Pacanaro, Denise Maria Christofolini, Leslie Domenici Kulikowski, et al.
Psychiatry Research|July 22, 2014
Expression profile of neurotransmitter receptor and regulatory genes in the prefrontal cortex of spontaneously hypertensive rats: relevance to neuropsychiatric disordersMarcos Leite Santoro, Camila Maurício Santos, Vanessa Kiyomi Ota, et al.
Molecular Cytogenetics|November 1, 2013
Complex small supernumerary marker chromosomes - an updateThomas Liehr, Sanja Cirkovic, Tanja Lalic, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletionRoberta Santos Guilherme, Karina Cunha Soares, Milena Simioni, et al.
Journal of the Endocrine Society|November 6, 2019
The Natural History of a Man With Ovotesticular 46,XX DSD Caused by a Novel 3-Mb 15q26.2 Deletion Containing <i>NR2F2</i> GeneGianna Carvalheira, Andrea M Malinverni, Mariana Moysés-Oliveira, et al.
Clinics (Sao Paulo, Brazil)|October 26, 2017
Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experienceÉvelin Aline Zanardo, Roberta Lelis Dutra, Flavia Balbo Piazzon, et al.
Schizophrenia Research|October 6, 2012
DRD1 rs4532 polymorphism: a potential pharmacogenomic marker for treatment response to antipsychotic drugsVanessa Kiyomi Ota, Letícia Nery Spíndola, Ary Gadelha, et al.
Pageof 9

Showing results (71-80 of 86) with videos related to

Sort By:
Pageof 9
Genetics Research|April 8, 2024
Variants in Candidate Genes for Phenotype Heterogeneity in Patients with the 22q11.2 Deletion SyndromeNatalia Nunes, Beatriz Carvalho Nunes, Malú Zamariolli, et al.
Journal of Intellectual Disabilities : JOID|September 30, 2009
Evaluation of clinical checklists for fragile X syndrome screening in Brazilian intellectually disabled males: proposal for a new screening toolDenise M Christofolini, Eduardo M Abbud, Monica V N Lipay, et al.
World Journal of Gastroenterology|December 7, 2016
Identification of <i>IL11RA</i> and <i>MELK</i> amplification in gastric cancer by comprehensive genomic profiling of gastric cancer cell linesDanielle Queiroz Calcagno, Sylvia Santomi Takeno, Carolina Oliveira Gigek, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
A rare case of trisomy 15pter-q21.2 due to a de novo marker chromosomeAde Nubia Xavier Pacanaro, Denise Maria Christofolini, Leslie Domenici Kulikowski, et al.
Psychiatry Research|July 22, 2014
Expression profile of neurotransmitter receptor and regulatory genes in the prefrontal cortex of spontaneously hypertensive rats: relevance to neuropsychiatric disordersMarcos Leite Santoro, Camila Maurício Santos, Vanessa Kiyomi Ota, et al.
Molecular Cytogenetics|November 1, 2013
Complex small supernumerary marker chromosomes - an updateThomas Liehr, Sanja Cirkovic, Tanja Lalic, et al.
American Journal of Medical Genetics. Part A|April 5, 2014
Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletionRoberta Santos Guilherme, Karina Cunha Soares, Milena Simioni, et al.
Journal of the Endocrine Society|November 6, 2019
The Natural History of a Man With Ovotesticular 46,XX DSD Caused by a Novel 3-Mb 15q26.2 Deletion Containing <i>NR2F2</i> GeneGianna Carvalheira, Andrea M Malinverni, Mariana Moysés-Oliveira, et al.
Clinics (Sao Paulo, Brazil)|October 26, 2017
Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experienceÉvelin Aline Zanardo, Roberta Lelis Dutra, Flavia Balbo Piazzon, et al.
Schizophrenia Research|October 6, 2012
DRD1 rs4532 polymorphism: a potential pharmacogenomic marker for treatment response to antipsychotic drugsVanessa Kiyomi Ota, Letícia Nery Spíndola, Ary Gadelha, et al.
Pageof 9