81
TITLE: Development of NIPBL locus-specific database using LOVD: from novel mutations to further genotype-phenotype correlations in Cornelia de Lange Syndrome
AUTHORS: Jorge Oliveira; Cristina Dias; Egbert Redeker; Eurico Costa; João Silva; Margarida R Lima; Johan T Den Dunnen; Rosário Santos;
PUBLISHED: 2010, SOURCE: Human Mutation
INDEXED IN: Handle
82
TITLE: Novel synonymous substitution in POMGNT1 promotes exon skipping in a patient with congenital muscular dystrophy  Full Text
AUTHORS: Jorge Oliveira; Isabel Soares Silva ; Ivo Fokkema; Ana Goncalves; Alexandra Cabral; Luisa Diogo; Lucia Galan; Antonio Guimaraes; Isabel Fineza; Johan T den Dunnen; Rosario Santos;
PUBLISHED: 2008, SOURCE: JOURNAL OF HUMAN GENETICS, VOLUME: 53, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
83
TITLE: Founder effect of a new DYSF exon 48-skipping mutation detected in seven Portuguese dysferlinopathy patients  Full Text
AUTHORS: Santos, R; Oliveira, J; Vieira, E; Coelho, T; Carneiro Leite, A; Evangelista, T; Fortuna, A; Geraldo, A; Luis, N; Guimaraes, A;
PUBLISHED: 2007, SOURCE: 12th International Congress of the World-Muscle-Society in NEUROMUSCULAR DISORDERS, VOLUME: 17, ISSUE: 9-10
INDEXED IN: WOS CrossRef
IN MY: ORCID
84
TITLE: Silent exonic substitution in POMGnT1 promotes exon skipping in a CMD patient  Full Text
AUTHORS: Oliveira, J; Soares Silva, I; Goncalves, A; Fokkema, I; Cabral, A; Diogo, L; Galan, L; Guimaraes, A; Fineza, I; den Durmen, J; Santos, R;
PUBLISHED: 2007, SOURCE: 12th International Congress of the World-Muscle-Society in NEUROMUSCULAR DISORDERS, VOLUME: 17, ISSUE: 9-10
INDEXED IN: WOS CrossRef
IN MY: ORCID
85
TITLE: Identification of a novel AluSx-mediated deletion of exon 3 in the SBDS gene in a patient with Shwachman-Diamond syndrome  Full Text
AUTHORS: Elisio Costa ; Frederico Duque; Jorge Oliveira; Paula Garcia; Isabel Goncalves; Luisa Diogo; Rosario Santos;
PUBLISHED: 2007, SOURCE: BLOOD CELLS MOLECULES AND DISEASES, VOLUME: 39, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 15
IN MY: ORCID
86
TITLE: Molecular study of portuguese patients with clinical diagnosis of Shwachman-Diamond syndrome
AUTHORS: Elísio Costa; Jorge M S M Oliveira; Emília Vieira; Paula Garcia; Isabel Gonçalves; Luisa Diogo; José Barbot; Rosário Santos;
PUBLISHED: 2007
INDEXED IN: Handle
Page 9 of 9. Total results: 87.