121
TITLE: Multicolour FISH versus array CGH techniques. Which to choose for the characterization of small supernumerary marker chromosomes?  Full Text
AUTHORS: Melo, J; Kosyakova, N; Liehr, T; Backx, L; Vermeesch, J; Carreira, I;
PUBLISHED: 2009, SOURCE: 7th European Cytogenetics Conference in CHROMOSOME RESEARCH, VOLUME: 17
INDEXED IN: WOS
122
TITLE: Mowat-Wilson syndrome: an underdiagnosed syndrome?  Full Text
AUTHORS: Engenheiro, E; Moller, RS; Pinto, M; Soares, G; Nikanorova, M; Carreira, IM; Ullmann, R; Tommerup, N; Tumer, Z;
PUBLISHED: 2008, SOURCE: CLINICAL GENETICS, VOLUME: 73, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef: 10
IN MY: ORCID
123
TITLE: Clastogenic effects of hexavalent chromium in a human bronchial epithelial cell line  Full Text
AUTHORS: Rodrigues, CF; Urbano, AM; Matoso, E; Carreira, IM; Alpoim, MC;
PUBLISHED: 2008, SOURCE: Joint Conference of the 33rd FEBS Congress/11th IUBMB Conference in FEBS JOURNAL, VOLUME: 275
INDEXED IN: WOS
124
TITLE: First prenatally detected small supernumerary neocentromeric derivative chromosome 13 resulting in a non-mosaic partial tetrasomy 13q
AUTHORS: Mascarenhas, A; Matoso, E; Saraiva, J; Toennies, H; Gerlach, A; Juliao, MJ; Melo, JB ; Carreira, IM;
PUBLISHED: 2008, SOURCE: CYTOGENETIC AND GENOME RESEARCH, VOLUME: 121, ISSUE: 3-4
INDEXED IN: Scopus WOS CrossRef: 5
IN MY: ORCID
125
TITLE: Psychological distress in pregnant women with insomnia
AUTHORS: Azevedo, M; Bos, S ; Pereira, A; Maia, B; Marques, M; Soares, M; Gomes, A ; Valente, J; Macedo, A;
PUBLISHED: 2008, SOURCE: 22nd Annual Meeting of the Associated-Professional-Sleep-Societies in SLEEP, VOLUME: 31
INDEXED IN: WOS
126
TITLE: Metabolite Profiling of Human Amniotic Fluid by Hyphenated Nuclear Magnetic Resonance Spectroscopy  Full Text
AUTHORS: Gonçalo Graça; Iola F Duarte; Brian J. Goodfellow; Isabel M Carreira; Ana Bela Couceiro; Maria do Rosário Domingues; Manfred Spraul; Li-Hong Tseng; Ana M Gil;
PUBLISHED: 2008, SOURCE: Analytical Chemistry - Anal. Chem., VOLUME: 80, ISSUE: 15
INDEXED IN: CrossRef: 29
IN MY: ORCID
127
TITLE: Cytogenetically invisible microdeletions involving PITX2 in Rieger syndrome  Full Text
AUTHORS: Engenheiro, E; Saraiva, J; Carreira, I; Ramos, L; Ropers, HH; Silva, E ; Tommerup, N; Tumer, Z;
PUBLISHED: 2007, SOURCE: CLINICAL GENETICS, VOLUME: 72, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 9
IN MY: ORCID
128
TITLE: Isodicentric Y and Y marker chromosomes in a female with up to 8 cell lines
AUTHORS: Carreira, IM; Melo, JB; Marques, B; Mirante, A; Simoes, L; Pires, M; Mendes, C; Matoso, E;
PUBLISHED: 2007, SOURCE: 6th European Cytogenetics Conference in CHROMOSOME RESEARCH, VOLUME: 15
INDEXED IN: WOS
129
TITLE: Three Unusual but Cytogenetically Similar Cases With up to Five Different Cell Lines Involving Structural and Numerical Abnormalities of Chromosome 18
AUTHORS: Carreira, IM; Mascarenhas, A; Matoso, E; Couceiro, AB; Ramos, L; Dufke, A; Mazauric, M; Stressig, R; Kosyakova, N; Melo, JB; Liehr, T;
PUBLISHED: 2007, SOURCE: Journal of Histochemistry and Cytochemistry, VOLUME: 55, ISSUE: 11
INDEXED IN: CrossRef: 5
IN MY: ORCID
130
TITLE: Detection of subtelomeric rearrangements by multiple subtelomeric probes in selected patients with unexplained mental retardation
AUTHORS: Marques M Carreira; Matoso, E; Portocarrero, A; Sousa, S; Venancio, M; Ramos, L; Saraiva, J;
PUBLISHED: 2005, SOURCE: CHROMOSOME RESEARCH, VOLUME: 13
INDEXED IN: WOS
Page 13 of 14. Total results: 134.