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Maria Isabel Melaragno

Showing results (41-50 of 86) with videos related to

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Plos One|January 10, 2013
Linkage replication for chromosomal region 13q32 in schizophrenia: evidence from a Brazilian pilot study on early onset schizophrenia familiesAry Gadelha, Vanessa Kiyomi Ota, Jose Paya Cano, et al.
American Journal of Medical Genetics. Part A|September 18, 2008
Pure duplication 1q41-qter: further delineation of trisomy 1q syndromesLeslie Domenici Kulikowski, Fernanda T S Bellucco, Sintia I Nogueira, et al.
Epigenetics & Chromatin|May 18, 2023
Premature ovarian insufficiency is associated with global alterations in the regulatory landscape and gene expression in balanced X-autosome translocationsAdriana Di-Battista, Bianca Pereira Favilla, Malú Zamariolli, et al.
European Journal of Medical Genetics|March 18, 2008
Atypical 22q11.2 deletion in a patient with DGS/VCFS spectrumSintia Iole Nogueira, April M Hacker, Fernanda T S Bellucco, et al.
American Journal of Medical Genetics. Part A|April 21, 2021
Novel MYT1 variants expose the complexity of oculo-auriculo-vertebral spectrum genetic mechanismsMalú Zamariolli, Bruna Burssed, Mariana Moysés-Oliveira, et al.
Gene|January 31, 2012
Cytogenomic characterization of an unexpected 17.6 Mb 9p deletion associated to a 14.8 Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotypeVera de Freitas Ayres Meloni, Flavia Balbo Piazzon, Maria de Fátima de Faria Soares, et al.
Clinical Immunology (Orlando, Fla.)|September 13, 2020
Lymphoproliferative disorder with polyautoimmunity and hypogammaglobulinemia: An unusual presentation of 22q11.2 deletion syndromeDiogo C Soares, Anelisa G Dantas, Marina C Matta, et al.
European Journal of Human Genetics : EJHG|February 1, 2019
Breakpoint mapping at nucleotide resolution in X-autosome balanced translocations associated with clinical phenotypesMariana Moysés-Oliveira, Adriana Di-Battista, Malú Zamariolli, et al.
Cytogenetic and Genome Research|March 15, 2022
Minimal Critical Region and Genes for a Typical Presentation of Langer-Giedion SyndromeBianca Pereira Favilla, Bruna Burssed, Érika Mitie Yamashiro Coelho, et al.
Psychiatry Research|October 12, 2013
Neurotransmitter receptor and regulatory gene expression in peripheral blood of Brazilian drug-naïve first-episode psychosis patients before and after antipsychotic treatmentVanessa Kiyomi Ota, Cristiano Noto, Ary Gadelha, et al.
Pageof 9

Showing results (41-50 of 86) with videos related to

Sort By:
Pageof 9
Plos One|January 10, 2013
Linkage replication for chromosomal region 13q32 in schizophrenia: evidence from a Brazilian pilot study on early onset schizophrenia familiesAry Gadelha, Vanessa Kiyomi Ota, Jose Paya Cano, et al.
American Journal of Medical Genetics. Part A|September 18, 2008
Pure duplication 1q41-qter: further delineation of trisomy 1q syndromesLeslie Domenici Kulikowski, Fernanda T S Bellucco, Sintia I Nogueira, et al.
Epigenetics & Chromatin|May 18, 2023
Premature ovarian insufficiency is associated with global alterations in the regulatory landscape and gene expression in balanced X-autosome translocationsAdriana Di-Battista, Bianca Pereira Favilla, Malú Zamariolli, et al.
European Journal of Medical Genetics|March 18, 2008
Atypical 22q11.2 deletion in a patient with DGS/VCFS spectrumSintia Iole Nogueira, April M Hacker, Fernanda T S Bellucco, et al.
American Journal of Medical Genetics. Part A|April 21, 2021
Novel MYT1 variants expose the complexity of oculo-auriculo-vertebral spectrum genetic mechanismsMalú Zamariolli, Bruna Burssed, Mariana Moysés-Oliveira, et al.
Gene|January 31, 2012
Cytogenomic characterization of an unexpected 17.6 Mb 9p deletion associated to a 14.8 Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotypeVera de Freitas Ayres Meloni, Flavia Balbo Piazzon, Maria de Fátima de Faria Soares, et al.
Clinical Immunology (Orlando, Fla.)|September 13, 2020
Lymphoproliferative disorder with polyautoimmunity and hypogammaglobulinemia: An unusual presentation of 22q11.2 deletion syndromeDiogo C Soares, Anelisa G Dantas, Marina C Matta, et al.
European Journal of Human Genetics : EJHG|February 1, 2019
Breakpoint mapping at nucleotide resolution in X-autosome balanced translocations associated with clinical phenotypesMariana Moysés-Oliveira, Adriana Di-Battista, Malú Zamariolli, et al.
Cytogenetic and Genome Research|March 15, 2022
Minimal Critical Region and Genes for a Typical Presentation of Langer-Giedion SyndromeBianca Pereira Favilla, Bruna Burssed, Érika Mitie Yamashiro Coelho, et al.
Psychiatry Research|October 12, 2013
Neurotransmitter receptor and regulatory gene expression in peripheral blood of Brazilian drug-naïve first-episode psychosis patients before and after antipsychotic treatmentVanessa Kiyomi Ota, Cristiano Noto, Ary Gadelha, et al.
Pageof 9