Análise de marcadores moleculares para o diagnóstico da síndrome de Williams-Beuren

by Roberta Lelis Dutra
Published 2011

Investigação da variação no número de cópias  genômicas (CNVs) em pacientes com anomalias congênitas e atraso de desenvolvimento neuropsicomotor (ADNPM) pela técnica de MLPA (Multi...

by Roberta Lelis Dutra
Published 2014

Investigation of Copy Number Variation in Children with Conotruncal Heart Defects

by Carla Marques Rondon Campos, Evelin Aline Zanardo, Roberta Lelis Dutra, Leslie Domenici Kulikowski, Chong Ae Kim
Published 2015-01-01

Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers

by Roberta Lelis Dutra, Patrícia de Campos Pieri, Ana Carolina Dias Teixeira, Rachel Sayuri Honjo, Debora Romeo Bertola, Chong Ae Kim
Published 2011-01-01

Estresse em crianças e adolescentes com Síndrome de Williams-Beuren em idade escolar

by Vera Alice Alcantara dos Santos Amaral, Michele Moreira Nunes, Rachel Sayuri Honjo, Roberta Lelis Dutra, Francisco Baptista Assumpção Jr, Chong Ae Kim

Corrigendum to “Williams-Beuren Syndrome: A Clinical Study of 55 Brazilian Patients and the Diagnostic Use of MLPA”

by Rachel Sayuri Honjo, Roberta Lelis Dutra, Erika Arai Furusawa, Evelin Aline Zanardo, Larissa Sampaio de Athayde Costa, Leslie Domenici Kulikowski, Debora Romeo Bertola, Chong Ae Kim
Published 2015-01-01

Williams-Beuren Syndrome: A Clinical Study of 55 Brazilian Patients and the Diagnostic Use of MLPA

by Rachel Sayuri Honjo, Roberta Lelis Dutra, Erika Arai Furusawa, Evelin Aline Zanardo, Larissa Sampaio de Athayde Costa, Leslie Domenici Kulikowski, Debora Romeo Bertola, Chong Ae Kim
Published 2015-01-01

FGFR4 profile as a prognostic marker in squamous cell carcinoma of the mouth and oropharynx.

by Roberta Lelis Dutra, Marcos Brasilino de Carvalho, Marcelo Dos Santos, Ana Maria da Cunha Mercante, Diana Gazito, Rafael de Cicco, Gencapo Group, Eloiza Helena Tajara, Iúri Drumond Louro, Adriana Madeira Álvares da Silva
Published 2012-01-01

Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experience

by Évelin Aline Zanardo, Roberta Lelis Dutra, Flavia Balbo Piazzon, Alexandre Torchio Dias, Gil Monteiro Novo-Filho, Amom Mendes Nascimento, Marília Moreira Montenegro, Jullian Gabriel Damasceno, Fabrícia Andreia Rosa Madia, Thaís Virgínia Moura Machado da Costa, Maria Isabel Melaragno, Chong Ae Kim, Leslie Domenici Kulikowski