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Sérgio Manuel Madeira Jorge Castedo
AuthID:
R-000-GF9
Publications
Confirmed
To Validate
Document Source:
All
Document Type:
All Document Types
Article (68)
Abstract (18)
Letter (7)
Note (5)
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Order:
Year Dsc
Year Asc
Cit. WOS Dsc
IF WOS Dsc
Cit. Scopus Dsc
IF Scopus Dsc
Title Asc
Title Dsc
Results:
10
20
30
40
50
Confirmed Publications: 98
51
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
52
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
:
108
IN MY:
ORCID
53
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
54
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
IN MY:
ORCID
55
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
56
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
57
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
58
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
59
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
60
TITLE:
IDENTIFICATION OF 2 DISTINCT REGIONS OF DELETION AT 6Q IN GASTRIC-CARCINOMA
AUTHORS:
QUEIMADO, L;
SERUCA, R
;
COSTAPEREIRA, A
;
CASTEDO, S
;
PUBLISHED:
1995
,
SOURCE:
GENES CHROMOSOMES & CANCER,
VOLUME:
14,
ISSUE:
1
INDEXED IN:
Scopus
WOS
CrossRef
:
37
IN MY:
ORCID
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