51
TITLE: MULTI-OMICS INTEGRATIVE PATHWAY ANALYSIS IN HEAD AND NECK SQUAMOUS CELL CARCINOMA  Full Text
AUTHORS: Esteves, L; Ribeiro, IP; Caramelo, F; Carreira, IM; Melo, JB;
PUBLISHED: 2021, SOURCE: 24th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 100, ISSUE: 4
INDEXED IN: WOS
IN MY: ORCID
52
TITLE: A PRENATAL CASE OF PARTIAL MONOSOMY 18 (q21.3-q23), RESULTING FROM A MATERNAL INSERTIONAL TRANSLOCATION ins(12;18) UNCOVERED BY ARRAY-CGH AND KARYOTYPING  Full Text
AUTHORS: Jardim, A; Ferreira, S; Matoso, E; Melo, JB; Carreira, IM;
PUBLISHED: 2021, SOURCE: 24th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 100, ISSUE: 4
INDEXED IN: WOS
IN MY: ORCID
53
TITLE: CELL-FREE DNA: A TOOL FOR THE DIAGNOSIS AND FOLLOW-UP OF ORAL CANCER?  Full Text
AUTHORS: Martins, I; Barroso, L; Tavares, I; Pires, LM; Marques, F; Melo, JB; Carreira, IM; Ribeiro, IP;
PUBLISHED: 2021, SOURCE: 24th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 100, ISSUE: 4
INDEXED IN: WOS
IN MY: ORCID
54
TITLE: A NIPT ANEUPLOIDY SUSPITION WITH NORMAL QF-PCR AND aCGH. KARYOTYPE GIVES THE ANSWER  Full Text
AUTHORS: Pinto, M; Pires, LM; Ferreira, S; Paiva, P; Jardim, A; Melo, JB; Carreira, IM;
PUBLISHED: 2021, SOURCE: 24th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 100, ISSUE: 4
INDEXED IN: WOS
IN MY: ORCID
55
TITLE: INCIDENTAL DETECTION OF MATERNAL Xp22.31 DELETIONS AND DUPLICATIONS IN NONINVASIVE PRENATAL TESTING  Full Text
AUTHORS: Pires, LM; Ferreira, SI; Almeida, P; Val, M; Lavoura, N; Ramos, F; Galhano, E; Melo, JB; Carreira, IM;
PUBLISHED: 2021, SOURCE: 24th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 100, ISSUE: 4
INDEXED IN: WOS
IN MY: ORCID
56
TITLE: SCRIB AND PIK3CB AS A PREDICTOR OF WORSE PROGNOSIS IN ORAL SQUAMOUS CELL CARCINOMAS  Full Text
AUTHORS: Ribeiro, IP; Esteves, L; Barroso, L; Marques, F; Caramelo, F; Melo, JB; Carreira, IM;
PUBLISHED: 2021, SOURCE: 24th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 100, ISSUE: 4
INDEXED IN: WOS
IN MY: ORCID
57
TITLE: DETECTION OF CHROMOSOME 3p DUPLICATION WITH ADJACENT TERMINAL DELETION IN PRENATAL DIAGNOSIS  Full Text
AUTHORS: Val, M; Ferreira, SI; Pires, LM; Lavoura, N; Mascarenhas, A; Pais, C; Carreira, IM; Melo, JB;
PUBLISHED: 2021, SOURCE: 24th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 100, ISSUE: 4
INDEXED IN: WOS
IN MY: ORCID
59
TITLE: Genomic characterisation of multiple myeloma: study of a Portuguese cohort
AUTHORS: Oliveira, AC; Ribeiro, IP; Pires, LM; Ana Cristina Gonçalves; Paiva, A; Geraldes, C; Roque, A; Sarmento Ribeiro, AB; de Melo, JB; Carreira, IM;
PUBLISHED: 2021, SOURCE: JOURNAL OF CLINICAL PATHOLOGY
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID
60
TITLE: Basal cell carcinomas of the scalp after radiotherapy for tinea capitis in childhood: A genetic and epigenetic study with comparison with basal cell carcinomas evolving in chronically sun-exposed areas  Full Text
AUTHORS: Cardoso, JC; Ribeiro, IP; Caramelo, F; Tellechea, O; de Melo, JB; Carreira, IM;
PUBLISHED: 2021, SOURCE: EXPERIMENTAL DERMATOLOGY, VOLUME: 30, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 5
IN MY: ORCID
Page 6 of 22. Total results: 212.