131
TITLE: A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability
AUTHORS: Ceroni, JRM; Dutra, RL; Honjo, RS; Llerena, JC; Acosta, AX; Medeiros, PFV; Galera, MF; Zanardo, EA; Piazzon, FB; Dias, AT; Novo, GM; Montenegro, MM; Madia, FAR; Bertola, DR; de Melo, JB; Kulikowski, LD; Kim, CA;
PUBLISHED: 2018, SOURCE: SCIENTIFIC REPORTS, VOLUME: 8, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID
132
TITLE: Genetics and myocardial infarction [Genética e enfarte do miocárdio]
AUTHORS: Melo, JB;
PUBLISHED: 2018, SOURCE: Revista Portuguesa de Cardiologia
INDEXED IN: Scopus
IN MY: ORCID
133
TITLE: Genetics and myocardial infarction
AUTHORS: Melo, JB;
PUBLISHED: 2018, SOURCE: REVISTA PORTUGUESA DE CARDIOLOGIA, VOLUME: 37, ISSUE: 9
INDEXED IN: WOS CrossRef: 1
IN MY: ORCID
134
TITLE: PATIENTS WITH RESISTANT HYPERTENSION AND NORMAL NOCTURNAL BLOOD PRESSURE DIPPING SHOW BETTER INFLAMMATION AND CARDIORESPIRATORY FITNESS
AUTHORS: Bastos, JM; Lopes, S; Ribau, V; Garcia, C; Bertoquini, S; Ribeiro, IP; Figueiredo, D; Viana, JL; Melo, JB; Alves, AJ; Ribeiro, F; Polonia, J;
PUBLISHED: 2018, SOURCE: 28th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH) in JOURNAL OF HYPERTENSION, VOLUME: 36, ISSUE: Supplement 1
INDEXED IN: WOS CrossRef
IN MY: ORCID
135
TITLE: Impact of the culturing conditions and culture age on the growth characteristics and genomic stability of BEAS-2B cells
AUTHORS: Abreu, PL; Ferreira, DC; Laranjeiro, AF; Mascarenhas, A; Pais, C; Melo, JB; Carreira, IM; Urbano, AM;
PUBLISHED: 2018, SOURCE: FREE RADICAL BIOLOGY AND MEDICINE, VOLUME: 120
INDEXED IN: WOS CrossRef
IN MY: ORCID
136
TITLE: Generation and characterization of a human iPS cell line from a patient-related control to study disease mechanisms associated with DAND5 p.R152H alteration
AUTHORS: Pars, S; Cristo, F; Inácio, JM; Rosas, G; Carreira, IM; Melo, JB; Mendes, P; Martins, DS; de Almeida, LP ; Maio, J; Anjos, R; Belo, JA;
PUBLISHED: 2018, SOURCE: STEM CELL RESEARCH, VOLUME: 29
INDEXED IN: Scopus WOS CrossRef: 3 Handle
IN MY: ORCID
137
TITLE: Five different 13q deletions in prenatal diagnosis
AUTHORS: Lavoura, N; Pires, LM; Ferreira, SI; Mascarenhas, A; Jardim, A; Pinto, MC; Pais, C; Galhano, E; Branco, M; Rei, AI; Gonçalves, H; Melo, JB; Carreira, IM;
PUBLISHED: 2018, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 26
INDEXED IN: WOS
IN MY: ORCID
138
TITLE: The importance of Array-CGH in the identification and characterization of 4p16.3 microdeletions in patients with Wolf-Hirschhorn Syndrome: A genotype/phenotype correlation attempt
AUTHORS: Pires, LM; Melo, JB; Ferreira, SI; Val, M; Lavoura, N; Jardim, A; Mascarenhas, A; Ramos, L; Saraiva, J; Carreira, IM;
PUBLISHED: 2018, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 26
INDEXED IN: WOS
IN MY: ORCID
139
TITLE: Gonadal mosaicism: its contribution for de novo events
AUTHORS: Carreira, IM; Pinto, MC; Jardim, A; Simoes, L; Paiva, P; Franco, S; Coelho, F; Oliveira, G; Melo, JB;
PUBLISHED: 2018, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 26
INDEXED IN: WOS
IN MY: ORCID
140
TITLE: <i>TBL1XR1</i> <i>de novo</i> deletion at 3(q26.32) in a boy with developmental delay, growth retardation and dysmorphisms
AUTHORS: Melo, JB; Ferreira, SI; Val; Maia, S; Carreira, IM;
PUBLISHED: 2018, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 26
INDEXED IN: WOS
IN MY: ORCID
Page 14 of 22. Total results: 212.