Sérgio Manuel Madeira Jorge Castedo


AuthID: R-000-GF9

Confirmed Publications: 98



31
TITLE: Frequency of NUP98-NSD1 fusion transcript in childhood acute myeloid leukaemia  Full Text
AUTHORS: Cerveira, N ; Correia, C; Doria, S ; Bizarro, S; Rocha, P; Gomes, P; Torres, L; Norton, L; Borges, BS; Castedo, S ; Teixeira, MR ;
PUBLISHED: 2003, SOURCE: LEUKEMIA, VOLUME: 17, ISSUE: 11
INDEXED IN: Scopus WOS CrossRef Unpaywall
IN MY: ORCID
32
TITLE: BRCA1 and BRCA2 mutations detected in breast/ovarian cancer patients of Portuguese origin
AUTHORS: Peixton, A; Salgueiro, N; Pereira, D; Rodrigues, H; Pereira, H; Regateiro, F; Teixeira, M; Castedo, S ;
PUBLISHED: 2002, SOURCE: INTERNATIONAL JOURNAL OF CANCER
INDEXED IN: WOS
33
TITLE: Terminal deletion of Xp22.3 associated with contiguous gene syndrome: Leri-Weill dyschondrosteosis, developmental delay, and ichthyosis  Full Text
AUTHORS: Vassal, H; Medeira, A; Cordeiro, I; Santos, HG; Castedo, S ; Saraiva, C; da Silva, PM; Monteiro, C;
PUBLISHED: 2001, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS, VOLUME: 99, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
34
TITLE: Detection of prognostic significant translocations in childhood acute lymphoblastic leukaemia by one-step multiplex reverse transcription polymerase chain reaction  Full Text
AUTHORS: Cerveira, N ; Ferreira, S; Doria, S ; Veiga, I; Ferreira, F; Martz, JM; Marques, M; Castedo, S ;
PUBLISHED: 2000, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 109, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 11
IN MY: ORCID
35
TITLE: Four novel MSH2 / MLH1 gene mutations in portuguese HNPCC families.  Full Text
AUTHORS: Isidro, G; Veiga, I; Matos, P ; Almeida, S; Bizarro, S; Marshall, B; Baptista, M; Leite, J; Regateiro, F; Soares, J; Castedo, S ; Boavida, MG;
PUBLISHED: 2000, SOURCE: Human mutation, VOLUME: 15, ISSUE: 1
INDEXED IN: Scopus CrossRef
IN MY: ORCID
36
TITLE: Pathological exon skipping in an HNPCC proband with MLHI splice acceptor site mutation  Full Text
AUTHORS: Clarke, LA ; Veiga, I; Isidro, G; Jordan, P ; Ramos, JS; Castedo, S ; Boavida, MG;
PUBLISHED: 2000, SOURCE: GENES CHROMOSOMES & CANCER, VOLUME: 29, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
37
TITLE: Significance of trisomy 7 and 12 in thyroid lesions with follicular differentiation: A cytogenetic and in situ hybridization study
AUTHORS: Rogue, L ; Serpa, A; Clode, A; Castedo, S ; Soares, J;
PUBLISHED: 1999, SOURCE: LABORATORY INVESTIGATION, VOLUME: 79, ISSUE: 4
INDEXED IN: Scopus WOS
38
TITLE: Tetrasomy of the short arm of chromosome 18. Two new cases
AUTHORS: Guilhas, C; Palmares, MC; Santos, MC; Cordeiro, I; Medeira, A; Castedo, S ; Rendeiro, P; Santos, HG;
PUBLISHED: 1999, SOURCE: CYTOGENETICS AND CELL GENETICS, VOLUME: 85, ISSUE: 1-2
INDEXED IN: WOS
39
TITLE: Williams-Beuren syndrome: 7q11.23 deletions and phenotypic variability in 50 cases
AUTHORS: Criado, B; Fernandes, R; Lima, MR; Mota, CR; Fortuna, A; Saraiva, J; Castedo, S ;
PUBLISHED: 1999, SOURCE: CYTOGENETICS AND CELL GENETICS, VOLUME: 85, ISSUE: 1-2
INDEXED IN: WOS
40
TITLE: 7q11.23 deletion in patients with suspected Williams syndrome: a FISH analysis of 30 cases  Full Text
AUTHORS: Criado, B; Fernandes, R; Lima, MR; Mota, CR; Fortuna, AM; Saraiva, J ; Castedo, S ;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6
INDEXED IN: WOS
Page 4 of 10. Total results: 98.

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