Sérgio Manuel Madeira Jorge Castedo


AuthID: R-000-GF9

Confirmed Publications: 101



51
TITLE: A FISH analysis of 14 patients with suspected Williams syndrome.
AUTHORS: Criado, B; Lima, MR; Mota, CR; Fortuna, AM; Saraiva, J; Santos, H; Cordeiro, I; Medeira, A; Castedo, S ;
PUBLISHED: 1997, SOURCE: CYTOGENETICS AND CELL GENETICS, VOLUME: 77, ISSUE: 1-2
INDEXED IN: WOS
52
TITLE: Angelman syndrome caused by loss of a marker chromosome: cytogenetic and fluorescence in situ hybridization analysis
AUTHORS: Arrieta, I; Criado, B; Nunez, T; Telez, M; Echarri, A; Martinez, B; Castedo, S ;
PUBLISHED: 1997, SOURCE: PSYCHIATRIC GENETICS, VOLUME: 7, ISSUE: 4
INDEXED IN: Scopus WOS
53
TITLE: Increased fetal nuchal translucency: possible involvement of early cardiac failure  Full Text
AUTHORS: Montenegro, N ; Matias, A ; Areias, JC ; Castedo, S ; Barros, H ;
PUBLISHED: 1997, SOURCE: ULTRASOUND IN OBSTETRICS & GYNECOLOGY, VOLUME: 10, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 107
IN MY: ORCID
54
TITLE: Prenatal diagnosis of partial trisomy 2q. Case report  Full Text
AUTHORS: Matos, A; Nogueira, A; Criado, B; Pereira, S; Castedo, S ; Montenegro, N ;
PUBLISHED: 1997, SOURCE: PRENATAL DIAGNOSIS, VOLUME: 17, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef: 13
IN MY: ORCID
55
TITLE: Probability tables for exclusion of mosaicism in prenatal diagnosis  Full Text
AUTHORS: SikkemaRaddatz, B; Castedo, S ; TeMeerman, GJ;
PUBLISHED: 1997, SOURCE: PRENATAL DIAGNOSIS, VOLUME: 17, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef
56
TITLE: Significant linkage disequilibrium between FRAXA locus and two polymorphic markers (FRAXAC1 and DXS548).
AUTHORS: Peixoto, AL; Santos, R; Seruca, R ; Carvalho, B; Amorim, Antonio ; Castedo, S ;
PUBLISHED: 1997, SOURCE: CYTOGENETICS AND CELL GENETICS, VOLUME: 77, ISSUE: 1-2
INDEXED IN: WOS
57
TITLE: Three novel APC gene mutations in Portuguese FAP kindreds
AUTHORS: Marshall, B; Isidro, G; Carvalhas, R; Veiga, I; Castedo, S ; Soares, J; Boavida, MG;
PUBLISHED: 1996, SOURCE: HUMAN MUTATION, VOLUME: 8, ISSUE: 4
INDEXED IN: WOS CrossRef: 2
58
TITLE: Bilateral split hand/foot malformation and inv(7)(p22q21.3).
AUTHORS: Cobben, JM; Verheij, JB; Eisma, WH; Robinson, PH; Zwierstra, RP; Leegte, B; Castedo, S ;
PUBLISHED: 1995, SOURCE: Journal of Medical Genetics, VOLUME: 32, ISSUE: 5
INDEXED IN: CrossRef: 11
IN MY: ORCID
59
TITLE: CYTOGENETIC FINDINGS IN 31 PAPILLARY THYROID CARCINOMAS
AUTHORS: ROGUE, L ; CLODE, AL; GOMES, P; ROSASANTOS, J; SOARES, J; CASTEDO, S ;
PUBLISHED: 1995, SOURCE: GENES CHROMOSOMES & CANCER, VOLUME: 13, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
60
TITLE: DETECTION OF NUMERICAL ALTERATIONS FOR CHROMOSOME-7 AND CHROMOSOME-12 IN BENIGN THYROID LESIONS BY IN-SITU HYBRIDIZATION - HISTOLOGICAL IMPLICATIONS
AUTHORS: CRIADO, B; BARROS, A ; SUIJKERBUIJK, RF; WEGHUIS, DO; SERUCA, R ; FONSECA, E ; CASTEDO, S ;
PUBLISHED: 1995, SOURCE: AMERICAN JOURNAL OF PATHOLOGY, VOLUME: 147, ISSUE: 1
INDEXED IN: Scopus WOS
Página 6 de 11. Total de resultados: 101.

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