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Isabel Melaragno

Showing results (21-30 of 87) with videos related to

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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.
Gene|June 6, 2019
Search for appropriate reference genes for quantitative reverse transcription PCR studies in somite, prosencephalon and heart of early mouse embryoMariana Moysés-Oliveira, Victória Cabral, Carolina Oliveira Gigek, et al.
Journal of Visualized Experiments : Jove|January 17, 2022
Technique for Obtaining Mesenchymal Stem Cell from Adipose Tissue and Stromal Vascular Fraction Characterization in Long-Term CryopreservationLeniza Pola-Silva, Fabio Xerfan Nahas, Flavia Nascimento, et al.
European Journal of Medical Genetics|January 30, 2022
CEDNIK syndrome in a Brazilian patient with compound heterozygous pathogenic variantsNatália Nunes, Malú Zamariolli, Anelisa Gollo Dantas, et al.
Molecular Genetics & Genomic Medicine|August 31, 2019
Rare single-nucleotide variants in oculo-auriculo-vertebral spectrum (OAVS)Malú Zamariolli, Mileny Colovati, Mariana Moysés-Oliveira, et al.
Genetics and Molecular Biology|December 11, 2020
Copy number variation (CNV) identification, interpretation, and database from Brazilian patientsVictória Cabral Silveira Monteiro de Godoy, Fernanda Teixeira Bellucco, Mileny Colovati, et al.
American Journal of Medical Genetics. Part A|April 29, 2021
Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effectsBianca Pereira Favilla, Vera Ayres Meloni, Ana Beatriz Perez, et al.
Arquivos Brasileiros De Cardiologia|July 1, 2009
22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotypeSintia Iole Nogueira Belangero, Fernanda T S Bellucco, Leslie Domenici Kulikowski, et al.
Cytogenetic and Genome Research|December 20, 2017
Deletion 21pterq22.11: Report of a Patient with Dysmorphic Features, Hypertonia, and Café-au-Lait Macules and Review of the LiteratureAndréa C M Malinverni, Érika M Yamashiro Coelho, Kelin Chen, et al.
Arquivos Brasileiros De Cardiologia|July 25, 2009
Interrupted aortic arch type B in A patient with cat eye syndromeSintia Iole Nogueira Belangero, Fernanda Teixeira da Silva Bellucco, Mirlene C S P Cernach, et al.
Pageof 9

Showing results (21-30 of 87) with videos related to

Sort By:
Pageof 9
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.
Gene|June 6, 2019
Search for appropriate reference genes for quantitative reverse transcription PCR studies in somite, prosencephalon and heart of early mouse embryoMariana Moysés-Oliveira, Victória Cabral, Carolina Oliveira Gigek, et al.
Journal of Visualized Experiments : Jove|January 17, 2022
Technique for Obtaining Mesenchymal Stem Cell from Adipose Tissue and Stromal Vascular Fraction Characterization in Long-Term CryopreservationLeniza Pola-Silva, Fabio Xerfan Nahas, Flavia Nascimento, et al.
European Journal of Medical Genetics|January 30, 2022
CEDNIK syndrome in a Brazilian patient with compound heterozygous pathogenic variantsNatália Nunes, Malú Zamariolli, Anelisa Gollo Dantas, et al.
Molecular Genetics & Genomic Medicine|August 31, 2019
Rare single-nucleotide variants in oculo-auriculo-vertebral spectrum (OAVS)Malú Zamariolli, Mileny Colovati, Mariana Moysés-Oliveira, et al.
Genetics and Molecular Biology|December 11, 2020
Copy number variation (CNV) identification, interpretation, and database from Brazilian patientsVictória Cabral Silveira Monteiro de Godoy, Fernanda Teixeira Bellucco, Mileny Colovati, et al.
American Journal of Medical Genetics. Part A|April 29, 2021
Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effectsBianca Pereira Favilla, Vera Ayres Meloni, Ana Beatriz Perez, et al.
Arquivos Brasileiros De Cardiologia|July 1, 2009
22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotypeSintia Iole Nogueira Belangero, Fernanda T S Bellucco, Leslie Domenici Kulikowski, et al.
Cytogenetic and Genome Research|December 20, 2017
Deletion 21pterq22.11: Report of a Patient with Dysmorphic Features, Hypertonia, and Café-au-Lait Macules and Review of the LiteratureAndréa C M Malinverni, Érika M Yamashiro Coelho, Kelin Chen, et al.
Arquivos Brasileiros De Cardiologia|July 25, 2009
Interrupted aortic arch type B in A patient with cat eye syndromeSintia Iole Nogueira Belangero, Fernanda Teixeira da Silva Bellucco, Mirlene C S P Cernach, et al.
Pageof 9