Publications by authors named "Roberta Dutra"

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Non-hermiticity in spintronics: oscillation death in coupled spintronic nano-oscillators through emerging exceptional points.
Steffen Wittrock, Salvatore Perna, Romain Lebrun, Katia Ho, Roberta Dutra

Nat Commun· February 2024

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Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experience.
Évelin Aline Zanardo, Roberta Lelis Dutra, Flavia Balbo Piazzon, Alexandre Torchio Dias, Gil Monteiro Novo-Filho

Clinics (Sao Paulo)· October 2017

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Subtelomeric Copy Number Variations: The Importance of 4p/4q Deletions in Patients with Congenital Anomalies and Developmental Disability.
Gil M Novo-Filho, Marília M Montenegro, Évelin A Zanardo, Roberta L Dutra, Alexandre T Dias

Cytogenet Genome Res· January 2017

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Post-mortem cytogenomic investigations in patients with congenital malformations.
Alexandre Torchio Dias, Évelin Aline Zanardo, Roberta Lelis Dutra, Flavia Balbo Piazzon, Gil Monteiro Novo-Filho

Exp Mol Pathol· August 2016

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Williams-Beuren Syndrome: A Clinical Study of 55 Brazilian Patients and the Diagnostic Use of MLPA.
Rachel Sayuri Honjo, Roberta Lelis Dutra, Erika Arai Furusawa, Evelin Aline Zanardo, Larissa Sampaio de Athayde Costa

Biomed Res Int· March 2016

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Corrigendum to "Williams-Beuren Syndrome: A Clinical Study of 55 Brazilian Patients and the Diagnostic Use of MLPA".
Rachel Sayuri Honjo, Roberta Lelis Dutra, Erika Arai Furusawa, Evelin Aline Zanardo, Larissa Sampaio de Athayde Costa

Biomed Res Int· February 2016

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Rare genomic rearrangement in a boy with Williams-Beuren syndrome associated to XYY syndrome and intriguing behavior.
Roberta L Dutra, Flavia B Piazzon, Évelin A Zanardo, Thais Virginia Moura Machado Costa, Marília M Montenegro

Am J Med Genet A· December 2015

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Cytogenomic delineation and clinical follow-up of 10 Brazilian patients with Pallister-Killian syndrome.
Larissa Sampaio de Athayde Costa, Aline C Zandona-Teixeira, Marilia M Montenegro, Alexandre T Dias, Roberta L Dutra

Mol Cytogenet· June 2015

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Investigation of copy number variation in children with conotruncal heart defects.
Carla Marques Rondon Campos, Evelin Aline Zanardo, Roberta Lelis Dutra, Leslie Domenici Kulikowski, Chong Ae Kim

Arq Bras Cardiol· January 2015

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Complex structural rearrangement features suggesting chromoanagenesis mechanism in a case of 1p36 deletion syndrome.
Évelin Aline Zanardo, Flavia Balbo Piazzon, Roberta Lelis Dutra, Alexandre Torchio Dias, Marília Moreira Montenegro

Mol Genet Genomics· December 2014

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Congenital Heart Disease as a Warning Sign for the Diagnosis of the 22q11.2 Deletion.
Marcília S Grassi, Cristina M A Jacob, Leslie D Kulikowski, Antonio C Pastorino, Roberta L Dutra

Arq Bras Cardiol· November 2014

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FGFR4 profile as a prognostic marker in squamous cell carcinoma of the mouth and oropharynx.
Roberta Lelis Dutra, Marcos Brasilino de Carvalho, Marcelo Dos Santos, Ana Maria da Cunha Mercante, Diana Gazito

PLoS One· May 2013

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Role of SNAP29, LZTR1 and P2RXL1 genes on immune regulation in a patient with atypical 0.5 Mb deletion in 22q11.2 region.
Diogo Cordeiro de Queiroz Soares, Roberta Lelis Dutra, Caio Robledo D'angioli Costa Quaio, Maria Isabel Melaragno, Leslie Domenici Kulikowski

Clin Immunol· October 2012

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Atypical deletion in Williams-Beuren syndrome critical region detected by MLPA in a patient with supravalvular aortic stenosis and learning difficulty.
Rachel Sayuri Honjo, Roberta Lelis Dutra, Michele Moreira Nunes, Israel Gomy, Leslie Domenici Kulikowski

J Genet Genomics· October 2012

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Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers.
Roberta Lelis Dutra, Patrícia de Campos Pieri, Ana Carolina Dias Teixeira, Rachel Sayuri Honjo, Debora Romeo Bertola

Clinics (Sao Paulo)· March 2012

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Copy number variation in Williams-Beuren syndrome: suitable diagnostic strategy for developing countries.
Roberta L Dutra, Rachel S Honjo, Leslie D Kulikowski, Fernanda M Fonseca, Patrícia C Pieri

BMC Res Notes· January 2012

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