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Alberto Manuel Barros da Silva

AuthID: R-000-KE6

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Confirmed Publications: 279

221

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

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222

TITLE: Study of genomic imprinting in spermatozoids from patients with oligozoospermia [Estudo do imprinting genómico em espermatozóides de pacientes com oligozoospermia]
AUTHORS: Marques, CJ ; Fernandes, S; Carvalho, F ; Silva, J; Sousa, M ; Barros, A ;
PUBLISHED: 2005, SOURCE: Revista Internacional de Andrologia, VOLUME: 3, ISSUE: 3

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223

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

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CrossRef: 36

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224

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

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225

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

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CrossRef: 29

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226

TITLE: CFTR gene mutations in congenital absence of vas deferens [Estudo das mutações do gene CFTR na ausência congénita dos canais deferentes]
AUTHORS: Grangeia, A ; Carvalho, F ; Sousa, M ; Barros, A ;
PUBLISHED: 2004, SOURCE: Arquivos de Medicina, VOLUME: 18, ISSUE: 1-2

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227

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

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228

TITLE: CYP21 gene mutations in Portuguese CAH patients
AUTHORS: Marques, CJ ; White, C; Fernandes, S; Carvalho, F ; Barros, A ; Witchel, SF; Pignatelli, D;
PUBLISHED: 2004, SOURCE: 12th International Congress of Endocrinology in PROCEEDINGS OF THE 12TH INTERNATIONAL CONGRESS OF ENDOCRINOLOGY

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229