Carreira, Isabel M.
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Name
Carreira, Isabel M.
Variants
Carreira, I.
Carreira, Isabel Marques
Carreira, Isabel Marques
Unidade de I&D
Ciência ID
Scopus Author ID
Researcher ID
Status
UC Researcher
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Type
Fulltext
Results 1-7 of 7 (Search time: 0.01 seconds).
Issue Date | Title | Author(s) | Type | Access | |
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1 | 2015 | Characterization of the genetic and epigenetic profile of tongue squamous cell carcinoma | Lisboa, Sofia Matos | masterThesis | openAccess |
2 | 2015 | Copy number variants prioritization after array-CGH analysis - a cohort of 1000 patients | Carreira, Isabel Marques ; Ferreira, Susana Isabel ; Matoso, Eunice ; Pires, Luís Miguel ; Ferrão, José ; Jardim, Ana ; Mascarenhas, Alexandra ; Pinto, Marta ; Lavoura, Nuno ; Pais, Claudia ; Paiva, Patrícia ; Simões, Lúcia ; Caramelo, Francisco ; Ramos, Lina ; Venâncio, Margarida ; Ramos, Fabiana; Beleza, Ana; Sá, Joaquim ; Saraiva, Jorge ; Melo, Joana Barbosa de | article | openAccess |
3 | 2015 | Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: the possible role for UBA2 gene | Melo, Joana B. ; Estevinho, Alexandra ; Saraiva, Jorge; Ramos, Lina ; Carreira, Isabel M. | article | openAccess |
4 | 19-Mar-2015 | Desequilíbrios genómicos nas patologias do desenvolvimento e do comportamento | Matoso, Eunice Maria Ruas de Campos | doctoralThesis | embargoedAccess |
5 | 2015 | High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia | Othman, Moneeb A. K. ; Melo, Joana B. ; Carreira, Isabel M. ; Rincic, Martina ; Glaser, Anita ; Grygalewicz, Beata; Gruhn, Bernd; Wilhelm, Kathleen; Rittscher, Katharina; Meyer, Britta; Silva, Maria Luiza Macedo; de Jesus Marques Salles, Terezinha; Liehr, Thomas | article | openAccess |
6 | 2015 | Isochromosome 17q in Chronic Lymphocytic Leukemia | Alhourani, Eyad ; Rincic, Martina ; Melo, Joana B. ; Carreira, Isabel M. ; Glaser, Anita ; Pohle, Beate; Schlie, Cordula; Liehr, Thomas | article | openAccess |
7 | 22-Aug-2015 | A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases | Vaz, Sara O. ; Pires, Renato ; Pires, Luís M. ; Carreira, Isabel M. ; Anjos, Rui ; Maciel, Paula ; Mota-Vieira, Luisa | article | openAccess |