Jorge Macedo Rocha


AuthID: R-000-7R2

Confirmed Publications: 92



71
TITLE: The phylogeography of Brazilian Y-chromosome lineages
AUTHORS: Carvalho Silva, DR; Santos, FR; Rocha, J ; Pena, SDJ;
PUBLISHED: 2001, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 68, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 246
IN MY: ORCID
72
TITLE: A novel alpha-1-antitrypsin r281del variant found in a population sample from the Basque country.  Full Text
AUTHORS: Seixas, S; Garcia, O; Amorim, Antonio ; Rocha, J ;
PUBLISHED: 2000, SOURCE: Human mutation, VOLUME: 15, ISSUE: 1
INDEXED IN: Scopus CrossRef: 3
IN MY: ORCID
73
74
TITLE: A novel alpha-1-antitrypsin P362H variant found in a population sample from São Tomé e Príncipe (Gulf of Guinea, West Africa)  Full Text
AUTHORS: Seixas, S ; Trovoada, MJ; Santos, MT; Rocha, J ;
PUBLISHED: 1999, SOURCE: Human Mutation, VOLUME: 13, ISSUE: 5
INDEXED IN: Scopus
IN MY: ORCID
75
TITLE: Adenosine deaminase polymorphisms at the protein and DNA levels
AUTHORS: Santos, F; Amorim, Antonio ; Rocha, J ; Kompf, J;
PUBLISHED: 1999, SOURCE: HUMAN BIOLOGY, VOLUME: 71, ISSUE: 6
INDEXED IN: Scopus WOS
IN MY: ORCID
76
77
TITLE: Identification in Portugal and Brazil of a mtDNA lineage containing a 9-bp triplication of the intergenic COII/tRNA(Lys) region
AUTHORS: Alves Silva, J; Guimaraes, PEM; Rocha, J ; Pena, SDJ; Prado, VF;
PUBLISHED: 1999, SOURCE: HUMAN HEREDITY, VOLUME: 49, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 4
IN MY: ORCID
78
79
TITLE: Molecular basis for arginase deficiency in Portugal: a novel R21X nonsense mutation detected in six pediatric patients with argininemia  Full Text
AUTHORS: Cardoso, ML; Rocha, J ; Martins, E; Vilarinho, L;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6
INDEXED IN: WOS
IN MY: ORCID
80
TITLE: alpha 1 anti-trypsin deficiency - A new M variant?
AUTHORS: Lopes, AI; Rocha, J ; Batista, A; daSilva, L; Salgueiro, C; deSousa, JS;
PUBLISHED: 1997, SOURCE: GUT, VOLUME: 41
INDEXED IN: WOS
IN MY: ORCID
Page 8 of 10. Total results: 92.

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