Zobrazeno 1 - 9
of 9
pro vyhledávání: '"M. Lurdes Pontes"'
Autor:
M. Lurdes Pontes, Rui Medeiros
Publikováno v:
Australian Journal of Forensic Sciences. 48:248-256
The aim of this work was to test a 52 SNP-plex in our laboratory in order to apply it in casework cases, namely in kinship involving relatives of the true father leading to low Parentage Index (PI) values, and in unusual cases such as paraffin-embedd
Autor:
Déborah Jamet, Barbara Lehner, Małgorzata Uhrynowska, Hubert Schrezenmeier, Paul V. Haydock, Erwin A. Scharberg, M. Lurdes Pontes, Ewa Brojer, Claude Férec, Eduard K. Petershofen, Zbigniew Celewicz, Thomasz Adamczyk, Katarzyna Guz, Christof Jungbauer, Sina Rothenberger, Peter Bugert, María S. Vitali, Andrea Doescher, Marzena Dębska, Simon Panzer, Ramin Lotfi, Agnieszka Orzińska, Manuel Fondevila, Hugo A. Guglielmone, Virginie Scotet, Adriana E. Oviedo, Naime Kömürcü, Christine Kroll, Dietmar Plonné, Russ Aldrich, Mirosław Wielgoś, Beate Eichelberger, Yann Fichou, Bernd Jahrsdörfer, Rui Medeiros, Maria Victoria Lareu, Cédric Le Maréchal, Thomas Müller, Gabi Rink, Carola Wieckhusen, María E. Bernardi
Publikováno v:
Transfusion Medicine and Hemotherapy. 42:409-411
Autor:
Déborah Jamet, Ramin Lotfi, Thomas Müller, Hugo A. Guglielmone, Hubert Schrezenmeier, Christine Kroll, Marzena Dębska, Manuel Fondevila, Paul V. Haydock, Katarzyna Guz, Gabi Rink, Erwin A. Scharberg, Małgorzata Uhrynowska, Ewa Brojer, Naime Kömürcü, María S. Vitali, Rui Medeiros, Andrea Doescher, Beate Eichelberger, Agnieszka Orzińska, Maria Victoria Lareu, Cédric Le Maréchal, Barbara Lehner, Claude Férec, Carola Wieckhusen, Russ Aldrich, Mirosław Wielgoś, M. Lurdes Pontes, Eduard K. Petershofen, María E. Bernardi, Thomasz Adamczyk, Sina Rothenberger, Dietmar Plonné, Christof Jungbauer, Zbigniew Celewicz, Bernd Jahrsdörfer, Simon Panzer, Yann Fichou, Virginie Scotet, Peter Bugert, Adriana E. Oviedo
Publikováno v:
Transfusion Medicine and Hemotherapy. 42:353-355
Publikováno v:
Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie. 42(6)
Background: DNA profiling with sets of highly polymorphic autosomal short tandem repeat (STR) markers has been applied in various aspects of human identification in forensic casework for nearly 20 years. However, in some cases of complex kinship inve
Autor:
M. Fátima Pinheiro, M. Lurdes Pontes
Publikováno v:
Forensic Science International: Genetics Supplement Series. 1:192-194
The non-recombining portion of the human Y (NRY) chromosome has various types of variation, including single nucleotide polymorphism (SNP). In spite of their low discrimination power, they provide a powerful and simple exclusion tool for forensic pur
Autor:
M.F. Pinheiro, M. Lurdes Pontes
Publikováno v:
Legal medicine (Tokyo, Japan). 16(2)
The use of autosomal single nucleotide polymorphisms (SNPs) for forensic research has been widely discussed in recent years, mainly because SNPs have important advantages compared to short tandem repeats (STRs). In this study a total of 131 non relat
Publikováno v:
Journal of forensic sciences. 52(2)
One hundred unrelated females and 100 unrelated males, autochthonous, healthy, from the North of Portugal. info:eu-repo/semantics/publishedVersion
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