Investigation of Copy Number Variation in Children with Conotruncal Heart Defects

Por Campos, Carla Marques Rondon, Zanardo, Evelin Aline, Dutra, Roberta Lelis, Kulikowski, Leslie Domenici, Kim, Chong Ae
Publicado no Arq Bras Cardiol (2015)

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

Por Dutra, Roberta Lelis, de Campos Pieri, Patrícia, Teixeira, Ana Carolina Dias, Honjo, Rachel Sayuri, Bertola, Debora Romeo, Kim, Chong Ae
Publicado em 2011

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

Por Honjo, Rachel Sayuri, Dutra, Roberta Lelis, Furusawa, Erika Arai, Zanardo, Evelin Aline, Costa, Larissa Sampaio de Athayde, Kulikowski, Leslie Domenici, Bertola, Debora Romeo, Kim, Chong Ae
Publicado no Biomed Res Int (2015)

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

Por Honjo, Rachel Sayuri, Dutra, Roberta Lelis, Furusawa, Erika Arai, Zanardo, Evelin Aline, Costa, Larissa Sampaio de Athayde, Kulikowski, Leslie Domenici, Bertola, Debora Romeo, Kim, Chong Ae
Publicado no Biomed Res Int (2015)

FGFR4 Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Mouth and Oropharynx

Por Dutra, Roberta Lelis, de Carvalho, Marcos Brasilino, dos Santos, Marcelo, Mercante, Ana Maria da Cunha, Gazito, Diana, de Cicco, Rafael, Group, GENCAPO, Tajara, Eloiza Helena, Louro, Iúri Drumond, da Silva, Adriana Madeira Álvares
Publicado em 2012

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

Por Zanardo, Évelin Aline, Dutra, Roberta Lelis, Piazzon, Flavia Balbo, Dias, Alexandre Torchio, Novo-Filho, Gil Monteiro, Nascimento, Amom Mendes, Montenegro, Marília Moreira, Damasceno, Jullian Gabriel, Madia, Fabrícia Andreia Rosa, da Costa, Thaís Virgínia Moura Machado, Melaragno, Maria Isabel, Kim, Chong Ae, Kulikowski, Leslie Domenici
Publicado no Clinics (Sao Paulo) (2017)