11
TITLE: Prevalence of X-aneuploidies and X-structural abnormalities in a Portuguese population with primary amenorrhea or premature ovarian insufficiency  Full Text
AUTHORS: Alexandra Estevinho; Ana R Neves; Jorge M Saraiva; Luis M Pires; Joana B Melo; Isabel M Carreira; Eunice Matoso;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
INDEXED IN: WOS
12
TITLE: Interstitial triplication 20p11.22p11.21, in a girl with development delay and vertebral anomalies, disclosed by array-CGH  Full Text
AUTHORS: Eunice Matoso; Lina Ramos; Jorge Saraiva; Alexandra Estevinho; Susana I Ferreira; Joana B Melo; Isabel M Carreira;
PUBLISHED: 2019, SOURCE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, ISSUE: 26
INDEXED IN: WOS
13
TITLE: Non-invasive allele-specific silencing therapy and biomarkers for Machado-Joseph disease
AUTHORS: Nobre, RJ; Saraiva, J; Fusco, C; Paixao, S; Santana, M; Petrella, L; Sereno, J; Castelhano, J; Castelo Branco, M; Sena Esteves, M; Pereira de Almeida, LP;
PUBLISHED: 2018, SOURCE: Conference on Changing the Face of Modern Medicine - Stem Cell and Gene Therapy in HUMAN GENE THERAPY, VOLUME: 29, ISSUE: 12
INDEXED IN: WOS
14
TITLE: Non-invasive AAV9-mediated silencing of mutant ataxin-3 alleviates motor and neuropathological deficits in a transgenic mouse model of Machado-Joseph disease
AUTHORS: Nobre, RJ; Saraiva, J; Fusco, C; Paixao, S; Santana, M; Sena Esteves, M; Almeida, LP;
PUBLISHED: 2016, SOURCE: Conference on Changing the Face of Modern Medicine - Stem Cells and Gene Therapy in HUMAN GENE THERAPY, VOLUME: 27, ISSUE: 11
INDEXED IN: WOS
15
TITLE: DVL1 Frameshift Mutations Clustering in the Penultimate Exon Cause Autosomal-Dominant Robinow Syndrome
AUTHORS: Janson White; Juliana F Mazzeu; Alexander Hoischen; Shalini N Jhangiani; Tomasz Gambin; Michele Calijorne Alcino; Samantha Penney; Jorge M Saraiva; Hanne Hove; Flemming Skovby; Hulya Kayserili; Elicia Estrella; Anneke T Vulto van Silfhout; Marloes Steehouwer; Donna M Muzny; Reid R Sutton; Richard A Gibbs; James R Lupski; Han G Brunner; Bregje W M van Bon; Claudia M B Carvalho; ...More
PUBLISHED: 2015, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 96, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
16
TITLE: Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: the possible role for UBA2 gene  Full Text
AUTHORS: Joana B Melo; Alexandra Estevinho; Jorge Saraiva; Lina Ramos; Isabel M Carreira;
PUBLISHED: 2015, SOURCE: MOLECULAR CYTOGENETICS, VOLUME: 8, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 9
17
TITLE: Genetic Counseling in Portugal: Education, Practice and a Developing Profession  Full Text
AUTHORS: Milena Paneque ; Alvaro Mendes ; Jorge Saraiva; Jorge Sequeiros;
PUBLISHED: 2015, SOURCE: JOURNAL OF GENETIC COUNSELING, VOLUME: 24, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 14
18
TITLE: 12q21.2q22 Deletion: A New Patient  Full Text
AUTHORS: Renata Oliveira; Cristina Pereira; Joana B Melo; Sandra Mesquita; Margarida Venancio; Isabel Marques Carreira; Jorge Saraiva;
PUBLISHED: 2015, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 167, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 1
20
TITLE: Intellectual Disability, Coarse Face, Relative Macrocephaly, and Cerebellar Hypotrophy in Two Sisters  Full Text
AUTHORS: Sergio B Sousa; Fabiana Ramos; Paula Garcia; Rui P Pais; Catarina Paiva; Philip L Beales; Gudrun E Moore; Jorge M Saraiva; Raoul C M Hennekam;
PUBLISHED: 2014, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 164, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 4
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