Susana Maria Gouveia Fernandes
AuthID: R-000-K31
41
TITLE: Unique t(Y;1)(q12;q12) reciprocal translocation with loss of the heterochromatic region of chromosome 1 in a male with azoospermia due to meiotic arrest: a case report
AUTHORS: Pinho, MJ; Neves, R; Costa, P; Ferras, C ; Sousa, M ; Alves, C; Almeida, C ; Fernandes, S; Silva, J; Ferras, L ; Barros, A ;
PUBLISHED: 2005, SOURCE: HUMAN REPRODUCTION, VOLUME: 20, ISSUE: 3
AUTHORS: Pinho, MJ; Neves, R; Costa, P; Ferras, C ; Sousa, M ; Alves, C; Almeida, C ; Fernandes, S; Silva, J; Ferras, L ; Barros, A ;
PUBLISHED: 2005, SOURCE: HUMAN REPRODUCTION, VOLUME: 20, ISSUE: 3
42
TITLE: A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens
AUTHORS: Grangeia, A ; Carvalho, F ; Fernandes, S; Silva, J; Sousa, M ; Barros, A ;
PUBLISHED: 2005, SOURCE: FERTILITY AND STERILITY, VOLUME: 83, ISSUE: 2
AUTHORS: Grangeia, A ; Carvalho, F ; Fernandes, S; Silva, J; Sousa, M ; Barros, A ;
PUBLISHED: 2005, SOURCE: FERTILITY AND STERILITY, VOLUME: 83, ISSUE: 2
43
TITLE: Cytogenetic and molecular characterization of Y dicentric chromosomes
AUTHORS: Doria, S ; Fernandes, S; Alves, C; Lima, V; Almeida, C; Moreira, L; Pereira, S; Sousa, M; Barros, A ;
PUBLISHED: 2005, SOURCE: CHROMOSOME RESEARCH, VOLUME: 13
AUTHORS: Doria, S ; Fernandes, S; Alves, C; Lima, V; Almeida, C; Moreira, L; Pereira, S; Sousa, M; Barros, A ;
PUBLISHED: 2005, SOURCE: CHROMOSOME RESEARCH, VOLUME: 13
INDEXED IN: 
WOS
WOS44
TITLE: In-vitro cocultures of the normal human seminiferous epithelium
AUTHORS: Silva, J; Alves, C; Fernandes, MS; Cremades, N; Ferras, C; Carvalho, F ; Fernandes, S; Sousa, M ; Teixeira da Silva, JT; Barros, A ;
PUBLISHED: 2003, SOURCE: HUMAN REPRODUCTION, VOLUME: 18
AUTHORS: Silva, J; Alves, C; Fernandes, MS; Cremades, N; Ferras, C; Carvalho, F ; Fernandes, S; Sousa, M ; Teixeira da Silva, JT; Barros, A ;
PUBLISHED: 2003, SOURCE: HUMAN REPRODUCTION, VOLUME: 18
INDEXED IN: WOS
WOS45
TITLE: High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia
AUTHORS: Fernandes, S; Huellen, K; Goncalves, J ; Dukal, H; Zeisler, J; De MEyts, ER; Skakkebaek, NE; Habermann, B; Krause, W; Sousa, M ; Barros, A ; Vogt, PH;
PUBLISHED: 2002, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 8, ISSUE: 3
AUTHORS: Fernandes, S; Huellen, K; Goncalves, J ; Dukal, H; Zeisler, J; De MEyts, ER; Skakkebaek, NE; Habermann, B; Krause, W; Sousa, M ; Barros, A ; Vogt, PH;
PUBLISHED: 2002, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 8, ISSUE: 3
46
TITLE: Preimplantation genetic diagnosis of familial amyloidotic polyneuropathy
AUTHORS: Carvalho, F ; Sousa, M ; Fernandes, S; Almeida, V ; Silva, J; Braga, J; Goncalves, J; Barros, A ;
PUBLISHED: 2001, SOURCE: HUMAN REPRODUCTION, VOLUME: 16
AUTHORS: Carvalho, F ; Sousa, M ; Fernandes, S; Almeida, V ; Silva, J; Braga, J; Goncalves, J; Barros, A ;
PUBLISHED: 2001, SOURCE: HUMAN REPRODUCTION, VOLUME: 16
INDEXED IN: WOS
WOS47
TITLE: Rapid screening protocol for complete AZFa deletions performed in men with complete germ cell aplasia (Sertoli cell-only syndrome)
AUTHORS: Vogt, PH; Kamp, C; Huellen, K; Fernandes, S; Schlegel, P; Kleiman, S; Krause, W; Kuepker, W; Schulze, W;
PUBLISHED: 2001, SOURCE: HUMAN REPRODUCTION, VOLUME: 16
AUTHORS: Vogt, PH; Kamp, C; Huellen, K; Fernandes, S; Schlegel, P; Kleiman, S; Krause, W; Kuepker, W; Schulze, W;
PUBLISHED: 2001, SOURCE: HUMAN REPRODUCTION, VOLUME: 16
INDEXED IN: WOS
WOS