Noninvasive prenatal paternity determination using microhaplotypes: a pilot study von Wang, Jaqueline Yu Ting, Whittle, Martin R., Puga, Renato David, Yambartsev, Anatoly, Fujita, Andre, Nakaya, Helder I.

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The 2000–2001 GEP–ISFG Collaborative Exercise on mtDNA: assessing the cause of unsuccessful mtDNA PCR amplification of hair shaft samples von Prieto, Lourdes, Montesino, Marta, Salas, Antonio, Alonso, Antonio, Albarrán, Cristina, Álvarez, Sara, Crespillo, Manuel, Di Lonardo, Ana M a, Doutremepuich, Christian, Fernández-Fernández, Isabel, de la Vega, Alberto González, Gusmão, Leonor, López, Carlos M, López-Soto, Manolo, Lorente, José A, Malaghini, Marcelo, Martı́nez, Carlos A, Modesti, Nidia M, Palacio, Ana M a, Paredes, Manuel, Pena, Sergio D.J, Pérez-Lezaun, Anna, Pestano, José J, Puente, Jorge, Sala, Andrea, Vide, M aConceiçao, Whittle, Martı́n R, Yunis, Juan J, Gómez, Josefina

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Comparison of southern Chinese Han and Brazilian Caucasian mutation rates at autosomal short tandem repeat loci used in human forensic genetics von Sun, Hongyu, Liu, Sujuan, Zhang, Yinming, Whittle, Martin R.

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Use of X-linked short tandem repeat loci in routine parentage casework von Silveira, Debora, Silva, Fabiana F., Jesus, Priscila R., Whittle, Martin R.

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Results of the 2003–2004 GEP-ISFG collaborative study on mitochondrial DNA: Focus on the mtDNA profile of a mixed semen-saliva stain von Crespillo, Manuel, Paredes, Miguel R., Prieto, Lourdes, Montesino, Marta, Salas, Antonio, Albarran, Cristina, V, Álvarez-Iglesias, Amorin, Antonio, Berniell-Lee, Gemma, Brehm, Antonio, Carril, Juan C., Corach, Daniel, Cuevas, Nerea, Di Lonardo, Ana M., Doutremepuich, Christian, Espinheira, Rosa M., Espinoza, Marta, Gómez, Felix, González, Alberto, Hernández, Alexis, Hidalgo, M., Jimenez, Magda, Leite, Fabio P.N., López, Ana M., López-Soto, Manuel, Lorente, Jose A., Pagano, Shintia, Palacio, Ana M., Pestano, José J., Pinheiro, Maria F., Raimondi, Eduardo, Ramón, M.M., Tovar, Florangel, Vidal-Rioja, Lidia, Vide, Maria C., Whittle, Martín R., Yunis, Juan J., Garcia-Hirschfel, Julia

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Mitochondrial DNA error prophylaxis: assessing the causes of errors in the GEP’02–03 proficiency testing trial von Salas, Antonio, Prieto, Lourdes, Montesino, Marta, Albarrán, Cristina, Arroyo, Eduardo, Paredes-Herrera, Miguel R., Di Lonardo, Ana Ma, Doutremepuich, Christian, Fernández-Fernández, Isabel, de la Vega, Alberto González, Alves, Cı́ntia, López, Carlos M., López-Soto, Manolo, Lorente, José A., Picornell, Antònia, Espinheira, Rosa M., Hernández, Alexis, Palacio, Ana Ma, Espinoza, Marta, Yunis, Juan J., Pérez-Lezaun, Anna, Pestano, José J., Carril, Juan Carlos, Corach, Daniel, Vide, Ma Conceiçao, Álvarez-Iglesias, V., Pinheiro, M.F., Whittle, Martı́n R., Brehm, Antonio, Gómez, Josefina

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Use of universal reporter primers in multiplex PCR of autosomal loci von Favaro, Elaine C., Sumita, Denilce R., Whittle, Martin R.

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An Unconditional Exact Test for the Hardy-Weinberg Equilibrium Law: Sample-Space Ordering Using the Bayes Factor von Montoya-Delgado, Luis E, Irony, Telba Z, de B. Pereira, Carlos A, Whittle, Martin R

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Results of the GEP-ISFG collaborative study on two Y-STRs tetraplexes: GEPY I (DYS461, GATA C4, DYS437 and DYS438) and GEPY II (DYS460, GATA A10, GATA H4 and DYS439) von Sánchez-Diz, Paula, Gusmão, Leonor, Beleza, Sandra, Benı́tez-Páez, Alfonso, Castro, Azucena, Garcı́a, Oscar, Solla, Lourdes Prieto, Geada, Helena, Martı́n, Pablo, Martı́nez-Jarreta, Begoña, de Fátima Pinheiro, Maria, Raimondi, Eduardo, Marı́a Silva de la Fuente, Sandra, Vide, Maria Conceição, Whittle, Martin R., Zarrabeitia, Marı́a Teresa, Carracedo, Angel, Amorim, António

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Results of the GEP-ISFG collaborative study on the Y chromosome STRs GATA A10, GATA C4, GATA H4, DYS437, DYS438, DYS439, DYS460 and DYS461: population data von Gusmão, Leonor, Sánchez-Diz, Paula, Alves, Cı́ntia, Quintáns, Beatriz, Garcı́a-Poveda, Emilio, Geada, Helena, Raimondi, Eduardo, Marı́a Silva de la Fuente, Sandra, Vide, Maria Conceição, Whittle, Martin R, Zarrabeitia, Marı́a Teresa, Carvalho, Mónica, Negreiros, Veranice, Prieto Solla, Lourdes, Riancho, José A, Campos-Sánchez, Rebeca, Vieira-Silva, Claúdia, Toscanini, Ulises, Amorim, António, Carracedo, Angel

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Development and use of a single-tube four dye, 21plex direct PCR autosomal STR loci amplification assay for human identification and relationship testing von Francischini, Carlos W., Sumita, Denilce R., Whittle, Martin R.

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Updated Brazilian genetic data, together with mutation rates, on 19 STR loci, including D10S1237 von Whittle, M.R., Romano, N.L., Negreiros, V.A.C.

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Use of matrix standards for new fluorophores in capillary sequencers von Whittle, Martin R., Favaro, Elaine C., Francischini, Carlos W., Sumita, Denilce R.

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Quadruplex real-time PCR for forensic DNA quantitation von Whittle, Martin R., Sumita, Denilce R.

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Comparison of STR loci profiles obtained from extracted FTA discs using different DNA polymerases von Sumita, Denilce R., Whittle, Martin R.

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Efficient mispriming during apolipoprotein E genotyping von Souza, Gabriela Merheb de Azevedo, Romano, Nara Lúcia, Whittle, Martin R.

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Efficient mispriming during apolipoprotein E genotyping Iniciação errônea eficiente durante a genotipagem de apolipoproteína E von Gabriela Merheb de Azevedo Souza, Nara Lúcia Romano, Martin R. Whittle

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Knobloch syndrome in a large Brazilian consanguineous family: Confirmation of autosomal recessive inheritance von Passos-Bueno, M. Rita, Marie, Suely K., Monteiro, Mario, Neustein, Isaac, Whittle, Martin R., Vainzof, Mariz, Zatz, Mayana

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Update on polycystic kidney disease (hereditary): genetic diagnosis and counseling von Bernardo, Wanderley M., Whittle, Martin R., Simões, Ricardo

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Fibroblasts in Pancreatic Ductal Adenocarcinoma: Biological Mechanisms and Therapeutic Targets von Whittle, Martin C., Hingorani, Sunil R.

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