41
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
42
TITLE: Analysis of FMR1 and flanking microsatellite markers in normal and fragile X chromosomes in Portugal: evidence for a "protector" haplotype  Full Text
AUTHORS: Peixoto, A; dos Santos, MR; Seruca, R ; Amorim, Antonio ; Castedo, S ;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 5
IN MY: ORCID
43
TITLE: Clinical and (cyto)genetic studies in chronic myeloid leukaemia (CML) with simple or complex variant Philadelphia translocations  Full Text
AUTHORS: Cerveira, N; Gomes, P; Correia, C; Bizarro, S; Veiga, I; Castro, I; Tavares, PFT; Castedo, S ;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6
INDEXED IN: WOS
44
TITLE: Cytogenetic and fluorescence in situ hybridization studies in a case of anaplastic thyroid carcinoma  Full Text
AUTHORS: Roque, L ; Soares, J; Castedo, S ;
PUBLISHED: 1998, SOURCE: CANCER GENETICS AND CYTOGENETICS, VOLUME: 103, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 11
IN MY: ORCID
45
TITLE: Cytogenetic investigations of 340 thyroid hyperplasias and adenomas revealing correlations between cytogenetic findings and histology  Full Text
AUTHORS: Belge, G; Rogue, L ; Soares, J; Bruckmann, S; Thode, B; Fonseca, E ; Clode, A; Bartnitzke, S; Castedo, S ; Bullerdiek, J;
PUBLISHED: 1998, SOURCE: CANCER GENETICS AND CYTOGENETICS, VOLUME: 101, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 59
IN MY: ORCID
46
TITLE: Follicular thyroid carcinoma: Chromosome analysis of 19 cases  Full Text
AUTHORS: Rogue, L ; Clode, A; Belge, G; Pinto, A; Bartnitzke, S; Santos, JR; Thode, B; Bullerdiek, J; Castedo, S ; Soares, J;
PUBLISHED: 1998, SOURCE: GENES CHROMOSOMES & CANCER, VOLUME: 21, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
47
TITLE: Haplotype analysis in fragile X and normal Portuguese populations  Full Text
AUTHORS: Peixoto, A; Santos, R; Seruca, R ; Amorim, Antonio ; Castedo, S ;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6
INDEXED IN: WOS
48
TITLE: Interstitial deletion of chromosome 21 resulting from segregation of a paternal balanced intrachromosomal insertion. Cytogenetic and FISH analysis  Full Text
AUTHORS: Carvalhas, R; Correia, H; Lanca, A; Smeets, D; Carreiro, M; Castedo, S ; Chaves, J;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6
INDEXED IN: WOS
49
TITLE: Results of a multicentric study of APC mutations in Portuguese FAP families  Full Text
AUTHORS: Isidro, G; Soares, J; Ramos, JS; Brito, MJ; Giria, J; Leite, J; Gorjao, R; Lemos, P; Regateiro, F; Marques, D; Rocha, A; Viana, L; Veiga, I; Castedo, S ; Boavida, MG;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6
INDEXED IN: WOS
50
TITLE: Three cases of mosaicism for balanced reciprocal translocations  Full Text
AUTHORS: Leegte, B; Sikkema Raddatz, B; Hordijk, R; Bouman, K; van Essen, T; Castedo, S ; de Jong, B;
PUBLISHED: 1998, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS, VOLUME: 79, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef
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