Eunice Maria Ruas de Campos Matoso
AuthID: R-002-RP8
11
TITLE: Inv21p12q22del21q22 and intellectual disability Full Text
AUTHORS: Renata Oliveira; Sofia Doria ; Carmen Madureira; Vera Lima ; Carolina Almeida ; Maria J Pinho; Ramalho C ; Eunice Matoso; Alberto Barros ; Isabel M Carreira ; Carla Pinto Moura ;
PUBLISHED: 2013, SOURCE: GENE, VOLUME: 517, ISSUE: 1
AUTHORS: Renata Oliveira; Sofia Doria ; Carmen Madureira; Vera Lima ; Carolina Almeida ; Maria J Pinho; Ramalho C ; Eunice Matoso; Alberto Barros ; Isabel M Carreira ; Carla Pinto Moura ;
PUBLISHED: 2013, SOURCE: GENE, VOLUME: 517, ISSUE: 1
12
TITLE: Cryptic 7q36.2q36.3 deletion causes multiple congenital eye anomalies and craniofacial dysmorphism Full Text
AUTHORS: Ana Beleza Meireles; Eunice Matoso; Lina Ramos; Joana B Melo ; Isabel M Carreira ; Eduardo D Silva ; Jorge M Saraiva;
PUBLISHED: 2013, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 161A, ISSUE: 3
AUTHORS: Ana Beleza Meireles; Eunice Matoso; Lina Ramos; Joana B Melo ; Isabel M Carreira ; Eduardo D Silva ; Jorge M Saraiva;
PUBLISHED: 2013, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 161A, ISSUE: 3
13
TITLE: Insertional Translocation Leading to a 4q13 Duplication Including the EPHA5 Gene in Two Siblings With Attention-Deficit Hyperactivity Disorder Full Text
AUTHORS: Eunice Matoso; Joana B Melo ; Susana I Ferreira; Ana Jardim; Teresa M Castelo; Anja Weise; Isabel M Carreira ;
PUBLISHED: 2013, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 161, ISSUE: 8
AUTHORS: Eunice Matoso; Joana B Melo ; Susana I Ferreira; Ana Jardim; Teresa M Castelo; Anja Weise; Isabel M Carreira ;
PUBLISHED: 2013, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 161, ISSUE: 8
14
TITLE: 3q13.31 microdeletion syndrome: report of a patient and further evidence for the involvement of ZBTB20 gene Full Text
AUTHORS: Joana Barbosa Melo; Susana Isabel Ferreira; Luis Miguel Pires; Alexandra Mascarenhas; Margarida Venancio; Eunice Matoso; Isabel Marques Carreira;
PUBLISHED: 2013, SOURCE: CHROMOSOME RESEARCH, VOLUME: 21
AUTHORS: Joana Barbosa Melo; Susana Isabel Ferreira; Luis Miguel Pires; Alexandra Mascarenhas; Margarida Venancio; Eunice Matoso; Isabel Marques Carreira;
PUBLISHED: 2013, SOURCE: CHROMOSOME RESEARCH, VOLUME: 21
INDEXED IN: 
WOS
WOS15
TITLE: Critical region in 2q31.2q32.3 deletion syndrome: Report of two phenotypically distinct patients, one with an additional deletion in Alagille syndrome region Full Text
AUTHORS: Susana Isabel Ferreira; Eunice Matoso; Margarida Venancio; Jorge Saraiva; Joana B Melo ; Isabel Marques Carreira ;
PUBLISHED: 2012, SOURCE: MOLECULAR CYTOGENETICS, VOLUME: 5, ISSUE: 1
AUTHORS: Susana Isabel Ferreira; Eunice Matoso; Margarida Venancio; Jorge Saraiva; Joana B Melo ; Isabel Marques Carreira ;
PUBLISHED: 2012, SOURCE: MOLECULAR CYTOGENETICS, VOLUME: 5, ISSUE: 1
16
TITLE: To be or not to be a CNV? How to interpret this question with MLPA Full Text
AUTHORS: Jose Ferrao; Eunice Matoso; Ana Beleza; Jorge Saraiva; Joana Melo; Isabel Carreira;
PUBLISHED: 2011, SOURCE: CHROMOSOME RESEARCH, VOLUME: 19
AUTHORS: Jose Ferrao; Eunice Matoso; Ana Beleza; Jorge Saraiva; Joana Melo; Isabel Carreira;
PUBLISHED: 2011, SOURCE: CHROMOSOME RESEARCH, VOLUME: 19
INDEXED IN: WOS
WOS17
TITLE: Cryptic 7q36.2-q36.3 deletion characterized by array-CGH associated with multiple congenital eye anomalies in a boy with normal psychomotor development Full Text
AUTHORS: Eunice Matoso; Ana Beleza Meireles; Renata Oliveira; Claudia Reis; Lina Ramos; Eduardo Silva; Ana Jardim; Alexandra Mascarenhas; Joana Melo; Isabel Carreira;
PUBLISHED: 2011, SOURCE: CHROMOSOME RESEARCH, VOLUME: 19
AUTHORS: Eunice Matoso; Ana Beleza Meireles; Renata Oliveira; Claudia Reis; Lina Ramos; Eduardo Silva; Ana Jardim; Alexandra Mascarenhas; Joana Melo; Isabel Carreira;
PUBLISHED: 2011, SOURCE: CHROMOSOME RESEARCH, VOLUME: 19
INDEXED IN: WOS
WOS18
TITLE: The hidden why Full Text
AUTHORS: Marta Pinto; Nuno Lavoura; Eunice Matoso; Eulalia Galhano; Lina Ramos; Isabel Carreira;
PUBLISHED: 2011, SOURCE: CHROMOSOME RESEARCH, VOLUME: 19
AUTHORS: Marta Pinto; Nuno Lavoura; Eunice Matoso; Eulalia Galhano; Lina Ramos; Isabel Carreira;
PUBLISHED: 2011, SOURCE: CHROMOSOME RESEARCH, VOLUME: 19
INDEXED IN: WOS
WOS19
TITLE: X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation Full Text
AUTHORS: Susana I Ferreira; Eunice Matoso; Marta Pinto; Joana Almeida; Thomas Liehr; Joana B Melo ; Isabel M Carreira ;
PUBLISHED: 2010, SOURCE: MOLECULAR CYTOGENETICS, VOLUME: 3, ISSUE: 1
AUTHORS: Susana I Ferreira; Eunice Matoso; Marta Pinto; Joana Almeida; Thomas Liehr; Joana B Melo ; Isabel M Carreira ;
PUBLISHED: 2010, SOURCE: MOLECULAR CYTOGENETICS, VOLUME: 3, ISSUE: 1
20
TITLE: Human bronchial epithelial cells malignantly transformed by hexavalent chromium exhibit an aneuploid phenotype but no microsatellite instability Full Text
AUTHORS: Rodrigues, CFD; Urbano, AM ; Matoso, E; Carreira, I ; Almeida, A; Santos, P; Maria Filomena Botelho ; Carvalho, L ; Alves, M ; Monteiro, C; Costa, AN; Moreno, V; Alpoim, MC;
PUBLISHED: 2009, SOURCE: MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, VOLUME: 670, ISSUE: 1-2
AUTHORS: Rodrigues, CFD; Urbano, AM ; Matoso, E; Carreira, I ; Almeida, A; Santos, P; Maria Filomena Botelho ; Carvalho, L ; Alves, M ; Monteiro, C; Costa, AN; Moreno, V; Alpoim, MC;
PUBLISHED: 2009, SOURCE: MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, VOLUME: 670, ISSUE: 1-2
