Osvaldo Moutinho Pereira Soares
AuthID: R-002-E61
11
TITLE: CASE REPORT: A RARE PARTIAL TRISOMY OF CHROMOSOME 15 Full Text
AUTHORS: Botelho, Pedro; Miranda, Maria; Martins, Marcia; Correia, Ana; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
AUTHORS: Botelho, Pedro; Miranda, Maria; Martins, Marcia; Correia, Ana; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
INDEXED IN: WOS
12
TITLE: A CASE REPORT OF ACUTE MYELOID LEUKEMIA WITH T(11;21)(Q13;Q22) DEMONSTRATING THE RELEVANCE OF CYTOGENETICS ANALYSIS Full Text
AUTHORS: Ribeiro, Ines Garcia; Souto, Marta; Seixas, Filipa; Cunha, Manuel; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
AUTHORS: Ribeiro, Ines Garcia; Souto, Marta; Seixas, Filipa; Cunha, Manuel; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
INDEXED IN: WOS
13
TITLE: COEXISTING JAK2 AND CALR MUTATIONS IN ESSENTIAL THROMBOCYTHEMIA: CASE REPORT Full Text
AUTHORS: Arantes, Regina; Li, Fernanda; Seixas, Filipa; Cunha, Manuel; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
AUTHORS: Arantes, Regina; Li, Fernanda; Seixas, Filipa; Cunha, Manuel; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
INDEXED IN: WOS
14
TITLE: 2Q32-Q33 DELETION SYNDROME: A DISTINCT SUBTYPE Full Text
AUTHORS: Souto, Marta; Martins, Marcia; Correia, Ana; Moutinho, Osvaldo; Leite, Rosario Pinto;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
AUTHORS: Souto, Marta; Martins, Marcia; Correia, Ana; Moutinho, Osvaldo; Leite, Rosario Pinto;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
INDEXED IN: WOS