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1
المؤلفون: Leonor Gusmão, Bruce Budowle, Carlos Vullo, Jennifer Churchill Cihlar, Reinhard Würzner, Seah Lay Hong, Claudia Barletta-Carrillo, Wiliam Usaquén, Bettina Zimmermann, Rosane Silva, Chantal Roth, Martin Bodner, Harald Niederstätter, Rodrigo S. Moura-Neto, L. Souto, Gabriela Huber, Robert Lagacé, Dayse A. Silva, Christina Strobl, Balázs Egyed, Walther Parson, Dean Herman Tineo, Andrea Casas-Vargas, Catarina Xavier, Katja Anslinger, Farida Alshamali, Lisa Schnaller, Sharon Wootton, Renata Jankova-Ajanovska, Nicole Huber
المصدر: Forensic Science International: Genetics. 42:244-251
مصطلحات موضوعية: Forensic Genetics, 0301 basic medicine, Mitochondrial DNA, Computational biology, Biology, DNA, Mitochondrial, Genome, DNA sequencing, Haplogroup, Pathology and Forensic Medicine, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, Genetics, Humans, 030216 legal & forensic medicine, Phylogeny, Sanger sequencing, Massive parallel sequencing, Phylogenetic tree, High-Throughput Nucleotide Sequencing, Sequence Analysis, DNA, Heteroplasmy, 030104 developmental biology, Haplotypes, Genome, Mitochondrial, symbols, Multiplex Polymerase Chain Reaction
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2
المؤلفون: Erika Maria Monteiro-Santos, Carlos A. Vaccaro, Ximena Taborga, Rui Manuel Reis, Claudia Barletta-Carrillo, Henrique de Campos Reis Galvão, Carlos Sarroca, L. Lena Morillas, Patricia Ashton-Prolla, Julio Sanchez de Monte, Maria del Carmen Castro-Mujica, Florencia Spirandelli, Benedito Mauro Rossi, Norma Teresa Rossi, Yenni Rodriguez, Mev Dominguez-Valentin, Enrique Spirandelli, Hélène Tubeuf, Pål Møller, Edenir Inêz Palmero, Eivind Hovig, Pablo Kalfayan, André Escremim de Paula, Patrik Wernhoff, Sergio Chialina, Sabrina Daniela da Silva, Florencia Neffa, Luis Gustavo Capochin Romagnolo, Karin Alvarez, Alexandra Martins, Constantino Dominguez-Barrera, Adriana Della Valle, Tamara Alejandra Piñero, Susana Revollo, Richard Quispe, Melva Gutiérrez Angulo, Francisco López-Köstner
المساهمون: Department of Genetics and Molecular Biology, Universidade Federal do Rio Grande do Sul [Porto Alegre] (UFRGS), Life and Health Sciences Research Institute [Braga] (ICVS), University of Minho [Braga], Institut Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ), Université Laval [Québec] (ULaval), Génomique et Médecine Personnalisée du Cancer et des Maladies Neuropsychiatriques (GPMCND), Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Génétique du cancer et des maladies neuropsychiatriques (GMFC), et. al., Universidade do Minho
المصدر: BMC Cancer, Vol 17, Iss 1, Pp 1-26 (2017)
BMC Cancer
BMC Cancer, BioMed Central, 2017, 17 (1), ⟨10.1186/s12885-017-3599-4⟩
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madridمصطلحات موضوعية: 0301 basic medicine, Male, Cancer Research, Pediatrics, [SDV]Life Sciences [q-bio], Medicina Básica [Ciências Médicas], DNA Mismatch Repair, 0302 clinical medicine, Risk Factors, PMS2, Medicine, Artikkel, Registries, ComputingMilieux_MISCELLANEOUS, medicine.diagnostic_test, Variants, Middle Aged, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Mmr, Lynch syndrome, Founder Effect, 3. Good health, Oncology, 030220 oncology & carcinogenesis, Population Surveillance, Ciências Médicas::Medicina Básica, Female, Research Article, Adult, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Genetic counseling, RNA Splicing, Genetic Counseling, lcsh:RC254-282, 03 medical and health sciences, Medisinske Fag: 700 [VDP], Internal medicine, parasitic diseases, Genetics, Humans, VDP::Medisinske Fag: 700, Genetic Predisposition to Disease, Genetic Testing, Germ-Line Mutation, Genetic testing, Science & Technology, business.industry, Microsatellite instability, Computational Biology, Genetic Variation, nutritional and metabolic diseases, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, MSH6, 030104 developmental biology, Latin America, MSH2, business, Founder effect
وصف الملف: application/pdf