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Maria Isabel Melaragno

Showing results (1-10 of 86) with videos related to

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Reproduction (Cambridge, England)|August 26, 2020
Genetics of premature ovarian insufficiency and the association with X-autosome translocationsAdriana Di-Battista, Mariana Moysés-Oliveira, Maria Isabel Melaragno
Molecular Cytogenetics|June 14, 2022
Mechanisms of structural chromosomal rearrangement formationBruna Burssed, Malú Zamariolli, Fernanda Teixeira Bellucco, et al.
Sleep Medicine Clinics|March 19, 2024
X-Chromosome Dependent Differences in the Neuronal Molecular Signatures and Their Implications in Sleep PatternsMariana Moysés-Oliveira, Bianca Pereira Favilla, Maria Isabel Melaragno, et al.
Molecular Genetics & Genomic Medicine|October 2, 2019
Malan syndrome in a patient with 19p13.2p13.12 deletion encompassing NFIX and CACNA1A genes: Case report and review of the literatureFernanda T Bellucco, Claudia B de Mello, Vera A Meloni, et al.
Molecular Syndromology|May 7, 2025
Clinical Characterization and Cytogenetic-Molecular Study of a Patient with a Ring Chromosome 12Vinícius Almeida da Nóbrega, Gabriella Rodrigues Dos Santos, Maria Isabel Melaragno, et al.
Medical Oncology (Northwood, London, England)|November 26, 2011
Additional chromosomal abnormalities detected by array comparative genomic hybridization in AMLAna Rosa S Costa, Sintia I Belangero, Maria Isabel Melaragno, et al.
American Journal of Medical Genetics. Part A|May 13, 2006
Hydrocephaly, penoscrotal transposition, and digital anomalies associated with de novo pseudodicentric rearranged chromosome 13 characterized by classical cytogenetic methods and mBAND analysisDenise Maria Christofolini, Maisa Yoshimoto, Jeremy A Squire, et al.
Molecular Syndromology|February 28, 2022
Multicentric Carpotarsal Osteolysis Syndrome in a Mother and Daughter with a <i>MAFB</i> Missense Variant and Natural History of the DiseaseKelin Chen, Malú Zamariolli, Maria de Fátima de Faria Soares, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 30, 2006
Detection of hidden Y mosaicism in Turner's syndrome: importance in the prevention of gonadoblastomaBianca Bianco, Mônica Vannucci Nunes Lipay, Maria Isabel Melaragno, et al.
American Journal of Medical Genetics. Part A|September 9, 2016
Unusual X-chromosome inactivation pattern in patients with Xp11.23-p11.22 duplication: Report and reviewAdriana Di-Battista, Vera Ayres Meloni, Magnus Dias da Silva, et al.
Pageof 9

Showing results (1-10 of 86) with videos related to

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Pageof 9
Reproduction (Cambridge, England)|August 26, 2020
Genetics of premature ovarian insufficiency and the association with X-autosome translocationsAdriana Di-Battista, Mariana Moysés-Oliveira, Maria Isabel Melaragno
Molecular Cytogenetics|June 14, 2022
Mechanisms of structural chromosomal rearrangement formationBruna Burssed, Malú Zamariolli, Fernanda Teixeira Bellucco, et al.
Sleep Medicine Clinics|March 19, 2024
X-Chromosome Dependent Differences in the Neuronal Molecular Signatures and Their Implications in Sleep PatternsMariana Moysés-Oliveira, Bianca Pereira Favilla, Maria Isabel Melaragno, et al.
Molecular Genetics & Genomic Medicine|October 2, 2019
Malan syndrome in a patient with 19p13.2p13.12 deletion encompassing NFIX and CACNA1A genes: Case report and review of the literatureFernanda T Bellucco, Claudia B de Mello, Vera A Meloni, et al.
Molecular Syndromology|May 7, 2025
Clinical Characterization and Cytogenetic-Molecular Study of a Patient with a Ring Chromosome 12Vinícius Almeida da Nóbrega, Gabriella Rodrigues Dos Santos, Maria Isabel Melaragno, et al.
Medical Oncology (Northwood, London, England)|November 26, 2011
Additional chromosomal abnormalities detected by array comparative genomic hybridization in AMLAna Rosa S Costa, Sintia I Belangero, Maria Isabel Melaragno, et al.
American Journal of Medical Genetics. Part A|May 13, 2006
Hydrocephaly, penoscrotal transposition, and digital anomalies associated with de novo pseudodicentric rearranged chromosome 13 characterized by classical cytogenetic methods and mBAND analysisDenise Maria Christofolini, Maisa Yoshimoto, Jeremy A Squire, et al.
Molecular Syndromology|February 28, 2022
Multicentric Carpotarsal Osteolysis Syndrome in a Mother and Daughter with a <i>MAFB</i> Missense Variant and Natural History of the DiseaseKelin Chen, Malú Zamariolli, Maria de Fátima de Faria Soares, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 30, 2006
Detection of hidden Y mosaicism in Turner's syndrome: importance in the prevention of gonadoblastomaBianca Bianco, Mônica Vannucci Nunes Lipay, Maria Isabel Melaragno, et al.
American Journal of Medical Genetics. Part A|September 9, 2016
Unusual X-chromosome inactivation pattern in patients with Xp11.23-p11.22 duplication: Report and reviewAdriana Di-Battista, Vera Ayres Meloni, Magnus Dias da Silva, et al.
Pageof 9