241
TITLE: Intersex. I. Genes involved in male sex determination [Intersexo. I - Genes envolvidos na determinação do sexo masculino]
AUTHORS: Sa, R ; Sousa, M ; Barros, A ;
PUBLISHED: 2005, SOURCE: Nascer e Crescer, VOLUME: 14, ISSUE: 4
INDEXED IN: Scopus
IN MY: ORCID
242
TITLE: Possible involvement of MLH3, MLH1 & MSH4 genes in prophase I progression in human spermatogenesis [Possível envolvimento dos genes MLH3, MLH1 e MSH4 na Progressão da Profase I na Esperatogénese Humana]
AUTHORS: Ferras, C ; Fernandes, S; Sousa, M ; Barros, A ;
PUBLISHED: 2005, SOURCE: Revista Iberoamericana de Fertilidad y Reproduccion Humana, VOLUME: 22, ISSUE: 1
INDEXED IN: Scopus
IN MY: ORCID
243
TITLE: Quantitative study of caspase-3 activity in semen and after swim-up preparation in relation to sperm quality
AUTHORS: Almeida, C ; Cardoso, MF ; Sousa, M ; Viana, P; Goncalves, A; Silva, J; Barros, A ;
PUBLISHED: 2005, SOURCE: HUMAN REPRODUCTION, VOLUME: 20, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 45
IN MY: ORCID
244
TITLE: Spermatid injection and beyond
AUTHORS: Sousa, M ; Cremades, N; Silva, J; Oliveira, C; Teixeira Silva, JM; Ferras, L; Viana, P; Sousa, S; Goncalves, A; Barros, A ;
PUBLISHED: 2005, SOURCE: 13th World Congress on In- Vitro Fertilization, Assisted Reproduction and Genetics in Proceedings of the 13th World Congress on In Vitro Fertilization, Assisted Reproduction & Genetics
INDEXED IN: WOS
247
TITLE: A moral case study for discussion: designer babies and tissue typing  Full Text
AUTHORS: Sousa, M ; Barros, A ;
PUBLISHED: 2004, SOURCE: REPRODUCTIVE BIOMEDICINE ONLINE, VOLUME: 9, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID
248
TITLE: AZF and DAZ gene copy-specific deletion analysis in maturation arrest and Sertoli cell-only syndrome
AUTHORS: Ferras, C ; Fernandes, S; Marques, CJ ; Carvalho, F ; Alves, C; Silva, J; Sousa, M ; Barros, A ;
PUBLISHED: 2004, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 10, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 29
IN MY: ORCID
249
250
TITLE: Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens
AUTHORS: Grangeia, A ; Niel, F; Carvalho, F ; Fernandes, S; Ardalan, A; Girodon, E; Silva, J; Ferras, L ; Sousa, M ; Barros, A ;
PUBLISHED: 2004, SOURCE: HUMAN REPRODUCTION, VOLUME: 19, ISSUE: 11
INDEXED IN: Scopus WOS CrossRef: 35
IN MY: ORCID
Page 25 of 34. Total results: 340.