Isabel Maria Marques Carreira


AuthID: R-000-6CD

Confirmed Publications: 45



41
TITLE: Portugal: The practice of medical genetics in Portugal
AUTHORS: Saraiva, JM; Pinto, MR; Monteiro, C; Marques, I ; Lima, MR; Medeira, A; Rendeiro, P;
PUBLISHED: 2001, SOURCE: Genetics in Medicine, VOLUME: 3, ISSUE: 3
INDEXED IN: Scopus
IN MY: ORCID
42
TITLE: Absence of a del(22q11) in a patient with the 3C (craniocerebellocardiac) syndrome
AUTHORS: Saraiva, JM; Matoso, E; Marques, I ;
PUBLISHED: 1998, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 35, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
43
TITLE: Craniosynostosis and chromosome 22q11 deletion (multiple letters) [1]
AUTHORS: Dean, JCS; De Silva, DC; Reardon, W; Di Rocco, M; Buocompagni, A; Picco, P; Vignola, S; Borrone, C; Gimelli, G; Hunter, A; Ryan, A; Goodship, JA; Wilson, DI; Saraiva, JM; Matoso, E; Marques, I ;
PUBLISHED: 1998, SOURCE: Journal of Medical Genetics, VOLUME: 35, ISSUE: 4
INDEXED IN: Scopus
IN MY: ORCID
44
TITLE: Trisomy 8 mosaicism: A further five cases illustrating marked clinical and cytogenetic variability
AUTHORS: Jordan, MA; Marques, I ; Rosendorff, J; De Ravel, TJL;
PUBLISHED: 1998, SOURCE: Genetic Counseling, VOLUME: 9, ISSUE: 2
INDEXED IN: Scopus
IN MY: ORCID
45
TITLE: Novel mutations and polymorphisms in the Fanconi anemia group C gene
AUTHORS: Gibson, RA; Morgan, NV; Goldstein, LH; Pearson, IC; Kesterton, IP; Foot, NJ; Jansen, S; Havenga, C; Pearson, T; De Ravel, TJ; Cohn, RJ; Marques, IM ; Dokal, I; Roberts, I; Marsh, J; Ball, S; David Milner, R; Llerena, JC; Samochatova, E; Mohan, SP; Vasudevan, P; Birjandi, F; Hajianpour, A; Murer Orlando, M; Mathew, CG; ...More
PUBLISHED: 1996, SOURCE: Human Mutation, VOLUME: 8, ISSUE: 2
INDEXED IN: Scopus CrossRef: 22
IN MY: ORCID
Page 5 of 5. Total results: 45.

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