المؤلفون: Pal Møller, Toni T. Seppälä, Aysel Ahadova, Emma J. Crosbie, Elke Holinski-Feder, Rodney Scott, Saskia Haupt, Gabriela Möslein, Ingrid Winship, Sanne W. Bajwa-ten Broeke, Kelly E. Kohut, Neil Ryan, Peter Bauerfeind, Laura E. Thomas, D. Gareth Evans, Stefan Aretz, Rolf H. Sijmons, Elizabeth Half, Karl Heinimann, Karoline Horisberger, Kevin Monahan, Christoph Engel, Giulia Martina Cavestro, Robert Fruscio, Naim Abu-Freha, Levi Zohar, Luigi Laghi, Lucio Bertario, Bernardo Bonanni, Maria Grazia Tibiletti, Leonardo S. Lino-Silva, Carlos Vaccaro, Adriana Della Valle, Benedito Mauro Rossi, Leandro Apolinário da Silva, Ivana Lucia de Oliveira Nascimento, Norma Teresa Rossi, Tadeusz Dębniak, Jukka-Pekka Mecklin, Inge Bernstein, Annika Lindblom, Lone Sunde, Sigve Nakken, Vincent Heuveline, John Burn, Eivind Hovig, Matthias Kloor, Julian R. Sampson, Mev Dominguez-Valentin, On behalf of the Prospective Lynch Syndrome Database (www.plsd.eu) and The European Hereditary Tumour Group (www.ehtg.org)

المصدر: Hereditary Cancer in Clinical Practice, Vol 21, Iss 1, Pp 1-12 (2023)

مصطلحات موضوعية: Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1897-4287

URL الوصول: https://doaj.org/article/952d37829e8040c192582717c1ee47f5

المؤلفون: Pål Møller, Toni Seppälä, James G. Dowty, Saskia Haupt, Mev Dominguez-Valentin, Lone Sunde, Inge Bernstein, Christoph Engel, Stefan Aretz, Maartje Nielsen, Gabriel Capella, Dafydd Gareth Evans, John Burn, Elke Holinski-Feder, Lucio Bertario, Bernardo Bonanni, Annika Lindblom, Zohar Levi, Finlay Macrae, Ingrid Winship, John-Paul Plazzer, Rolf Sijmons, Luigi Laghi, Adriana Della Valle, Karl Heinimann, Elizabeth Half, Francisco Lopez-Koestner, Karin Alvarez-Valenzuela, Rodney J. Scott, Lior Katz, Ido Laish, Elez Vainer, Carlos Alberto Vaccaro, Dirce Maria Carraro, Nathan Gluck, Naim Abu-Freha, Aine Stakelum, Rory Kennelly, Des Winter, Benedito Mauro Rossi, Marc Greenblatt, Mabel Bohorquez, Harsh Sheth, Maria Grazia Tibiletti, Leonardo S. Lino-Silva, Karoline Horisberger, Carmen Portenkirchner, Ivana Nascimento, Norma Teresa Rossi, Leandro Apolinário da Silva, Huw Thomas, Attila Zaránd, Jukka-Pekka Mecklin, Kirsi Pylvänäinen, Laura Renkonen-Sinisalo, Anna Lepisto, Päivi Peltomäki, Christina Therkildsen, Lars Joachim Lindberg, Ole Thorlacius-Ussing, Magnus von Knebel Doeberitz, Markus Loeffler, Nils Rahner, Verena Steinke-Lange, Wolff Schmiegel, Deepak Vangala, Claudia Perne, Robert Hüneburg, Aída Falcón de Vargas, Andrew Latchford, Anne-Marie Gerdes, Ann-Sofie Backman, Carmen Guillén-Ponce, Carrie Snyder, Charlotte K. Lautrup, David Amor, Edenir Palmero, Elena Stoffel, Floor Duijkers, Michael J. Hall, Heather Hampel, Heinric Williams, Henrik Okkels, Jan Lubiński, Jeanette Reece, Joanne Ngeow, Jose G. Guillem, Julie Arnold, Karin Wadt, Kevin Monahan, Leigha Senter, Lene J. Rasmussen, Liselotte P. van Hest, Luigi Ricciardiello, Maija R. J. Kohonen-Corish, Marjolijn J. L. Ligtenberg, Melissa Southey, Melyssa Aronson, Mohd N. Zahary, N. Jewel Samadder, Nicola Poplawski, Nicoline Hoogerbrugge, Patrick J. Morrison, Paul James, Grant Lee, Rakefet Chen-Shtoyerman, Ravindran Ankathil, Rish Pai, Robyn Ward, Susan Parry, Tadeusz Dębniak, Thomas John, Thomas van Overeem Hansen, Trinidad Caldés, Tatsuro Yamaguchi, Verónica Barca-Tierno, Pilar Garre, Giulia Martina Cavestro, Jürgen Weitz, Silke Redler, Reinhard Büttner, Vincent Heuveline, John L. Hopper, Aung Ko Win, Noralane Lindor, Steven Gallinger, Loïc Le Marchand, Polly A. Newcomb, Jane Figueiredo, Daniel D. Buchanan, Stephen N. Thibodeau, Sanne W. ten Broeke, Eivind Hovig, Sigve Nakken, Marta Pineda, Nuria Dueñas, Joan Brunet, Kate Green, Fiona Lalloo, Katie Newton, Emma J. Crosbie, Miriam Mints, Douglas Tjandra, Florencia Neffa, Patricia Esperon, Revital Kariv, Guy Rosner, Walter Hernán Pavicic, Pablo Kalfayan, Giovana Tardin Torrezan, Thiago Bassaneze, Claudia Martin, Gabriela Moslein, Aysel Ahadova, Matthias Kloor, Julian R. Sampson, Mark A. Jenkins, The European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC)

المصدر: Hereditary Cancer in Clinical Practice, Vol 20, Iss 1, Pp 1-11 (2022)

مصطلحات موضوعية: Lynch Syndrome, Epidemiology, Prevention, Penetrance, Colorectal cancer, Segregation analysis, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1897-4287

URL الوصول: https://doaj.org/article/b931c1477d4f40ef8fbc4e978abfdf69

المؤلفون: Juan Llerena, Chong Ae Kim, Virginia Fano, Pablo Rosselli, Paulo Ferrez Collett-Solberg, Paula Frassinetti Vasconcelos de Medeiros, Mariana del Pino, Débora Bertola, Charles Marques Lourenço, Denise Pontes Cavalcanti, Têmis Maria Félix, Antonio Rosa-Bellas, Norma Teresa Rossi, Fanny Cortes, Flávia Abreu, Nicolette Cavalcanti, Maria Cecilia Hervias Ruz, Wagner Baratela

المصدر: BMC Pediatrics, Vol 22, Iss 1, Pp 1-13 (2022)

مصطلحات موضوعية: Dwarfism, Management, Medical practice, FGFR3, Bone dysplasia, Guideline, Pediatrics, RJ1-570

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1471-2431

URL الوصول: https://doaj.org/article/6cb774ce002b42298b2e3017d9bdf78b

المؤلفون: Claudia Alejandra Martin, Lourdes Suárez Villasmil, Adela Sembaj, Fabian Gomez Balangione, Silvia Zunino, Cecilia del Carmen Montes, Adriana Borello, Andres Del Castillo, Maximiliano Zeballos, Norma Teresa Rossi

المصدر: Revista de la Facultad de Ciencias Médicas de Córdoba, Vol 79, Iss 3 (2022)

مصطلحات موضوعية: genes brca1, genes brca2, neoplasias de la mama, neoplasias ováricas, Medicine, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://revistas.unc.edu.ar/index.php/med/article/view/34533; https://doaj.org/toc/0014-6722; https://doaj.org/toc/1853-0605

URL الوصول: https://doaj.org/article/b6406ad8074744728120738fd69eeed7

المؤلفون: Benedito Mauro Rossi, Edenir Inêz Palmero, Francisco López-Kostner, Carlos Sarroca, Carlos Alberto Vaccaro, Florencia Spirandelli, Patricia Ashton-Prolla, Yenni Rodriguez, Henrique de Campos Reis Galvão, Rui Manuel Reis, André Escremim de Paula, Luis Gustavo Capochin Romagnolo, Karin Alvarez, Adriana Della Valle, Florencia Neffa, Pablo German Kalfayan, Enrique Spirandelli, Sergio Chialina, Melva Gutiérrez Angulo, Maria del Carmen Castro-Mujica, Julio Sanchez de Monte, Richard Quispe, Sabrina Daniela da Silva, Norma Teresa Rossi, Claudia Barletta-Carrillo, Susana Revollo, Ximena Taborga, L. Lena Morillas, Hélène Tubeuf, Erika Maria Monteiro-Santos, Tamara Alejandra Piñero, Constantino Dominguez-Barrera, Patrik Wernhoff, Alexandra Martins, Eivind Hovig, Pål Møller, Mev Dominguez-Valentin

المصدر: BMC Cancer, Vol 17, Iss 1, Pp 1-26 (2017)

مصطلحات موضوعية: Lynch syndrome, Mmr, Latin America, Variants, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s12885-017-3599-4; https://doaj.org/toc/1471-2407

URL الوصول: https://doaj.org/article/1c493e85a2f64dbc8249789857b5f939

المؤلفون: Mev Dominguez-Valentin, Saskia Haupt, Toni T. Seppälä, Julian R. Sampson, Lone Sunde, Inge Bernstein, Mark A. Jenkins, Christoph Engel, Stefan Aretz, Maartje Nielsen, Gabriel Capella, Francesc Balaguer, Dafydd Gareth Evans, John Burn, Elke Holinski-Feder, Lucio Bertario, Bernardo Bonanni, Annika Lindblom, Zohar Levi, Finlay Macrae, Ingrid Winship, John-Paul Plazzer, Rolf Sijmons, Luigi Laghi, Adriana Della Valle, Karl Heinimann, Tadeusz Dębniak, Robert Fruscio, Francisco Lopez-Koestner, Karin Alvarez-Valenzuela, Lior H. Katz, Ido Laish, Elez Vainer, Carlos Vaccaro, Dirce Maria Carraro, Kevin Monahan, Elizabeth Half, Aine Stakelum, Des Winter, Rory Kennelly, Nathan Gluck, Harsh Sheth, Naim Abu-Freha, Marc Greenblatt, Benedito Mauro Rossi, Mabel Bohorquez, Giulia Martina Cavestro, Leonardo S. Lino-Silva, Karoline Horisberger, Maria Grazia Tibiletti, Ivana do Nascimento, Huw Thomas, Norma Teresa Rossi, Leandro Apolinário da Silva, Attila Zaránd, Juan Ruiz-Bañobre, Vincent Heuveline, Jukka-Pekka Mecklin, Kirsi Pylvänäinen, Laura Renkonen-Sinisalo, Anna Lepistö, Päivi Peltomäki, Christina Therkildsen, Mia Gebauer Madsen, Stefan Kobbelgaard Burgdorf, John L. Hopper, Aung Ko Win, Robert W. Haile, Noralane Lindor, Steven Gallinger, Loïc Le Marchand, Polly A. Newcomb, Jane Figueiredo, Daniel D. Buchanan, Stephen N. Thibodeau, Magnus von Knebel Doeberitz, Markus Loeffler, Nils Rahner, Evelin Schröck, Verena Steinke-Lange, Wolff Schmiegel, Deepak Vangala, Claudia Perne, Robert Hüneburg, Silke Redler, Reinhard Büttner, Jürgen Weitz, Marta Pineda, Nuria Duenas, Joan Brunet Vidal, Leticia Moreira, Ariadna Sánchez, Eivind Hovig, Sigve Nakken, Kate Green, Fiona Lalloo, James Hill, Emma Crosbie, Miriam Mints, Yael Goldberg, Douglas Tjandra, Sanne W. ten Broeke, Revital Kariv, Guy Rosner, Suresh H. Advani, Lidiya Thomas, Pankaj Shah, Mithun Shah, Florencia Neffa, Patricia Esperon, Walter Pavicic, Giovana Tardin Torrezan, Thiago Bassaneze, Claudia Alejandra Martin, Gabriela Moslein, Pål Moller

المساهمون: Dominguez-Valentin, M, Haupt, S, Seppälä, T, Sampson, J, Sunde, L, Bernstein, I, Jenkins, M, Engel, C, Aretz, S, Nielsen, M, Capella, G, Balaguer, F, Evans, D, Burn, J, Holinski-Feder, E, Bertario, L, Bonanni, B, Lindblom, A, Levi, Z, Macrae, F, Winship, I, Plazzer, J, Sijmons, R, Laghi, L, Della Valle, A, Heinimann, K, Dębniak, T, Fruscio, R, Lopez-Koestner, F, Alvarez-Valenzuela, K, Katz, L, Laish, I, Vainer, E, Vaccaro, C, Carraro, D, Monahan, K, Half, E, Stakelum, A, Winter, D, Kennelly, R, Gluck, N, Sheth, H, Abu-Freha, N, Greenblatt, M, Rossi, B, Bohorquez, M, Cavestro, G, Lino-Silva, L, Horisberger, K, Tibiletti, M, Nascimento, I, Thomas, H, Rossi, N, Apolinário da Silva, L, Zaránd, A, Ruiz-Bañobre, J, Heuveline, V, Mecklin, J, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepistö, A, Peltomäki, P, Therkildsen, C, Madsen, M, Burgdorf, S, Hopper, J, Win, A, Haile, R, Lindor, N, Gallinger, S, Le Marchand, L, Newcomb, P, Figueiredo, J, Buchanan, D, Thibodeau, S, von Knebel Doeberitz, M, Loeffler, M, Rahner, N, Schröck, E, Steinke-Lange, V, Schmiegel, W, Vangala, D, Perne, C, Hüneburg, R, Redler, S, Büttner, R, Weitz, J, Pineda, M, Duenas, N, Vidal, J, Moreira, L, Sánchez, A, Hovig, E, Nakken, S, Green, K, Lalloo, F, Hill, J, Crosbie, E, Mints, M, Goldberg, Y

المصدر: Dominguez-Valentin, M, Haupt, S, Seppälä, T T, Sampson, J R, Sunde, L, Bernstein, I, Jenkins, M A, Engel, C, Aretz, S, Nielsen, M, Capella, G, Balaguer, F, Evans, D G, Burn, J, Holinski-Feder, E, Bertario, L, Bonanni, B, Lindblom, A, Levi, Z, Macrae, F, Winship, I, Plazzer, J-P, Sijmons, R, Laghi, L, Della Valle, A, Heinimann, K, Dębniak, T, Fruscio, R, Lopez-Koestner, F, Alvarez-Valenzuela, K, Katz, L H, Laish, I, Vainer, E, Vaccaro, C, Carraro, D M, Monahan, K, Half, E, Stakelum, A, Winter, D, Kennelly, R, Gluck, N, Sheth, H, Abu-Freha, N, Greenblatt, M, Rossi, B M, Bohorquez, M, Cavestro, G M, Lino-Silva, L S, Horisberger, K, Tibiletti, M G, Nascimento, I D, Thomas, H, Rossi, N T, Apolinário da Silva, L, Zaránd, A, Ruiz-Bañobre, J, Heuveline, V, Mecklin, J-P, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepistö, A, Peltomäki, P, Therkildsen, C, Madsen, M G, Burgdorf, S K, Hopper, J L, Win, A K, Haile, R W, Lindor, N, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J, Buchanan, D D, Thibodeau, S N, von Knebel Doeberitz, M, Loeffler, M, Rahner, N, Schröck, E, Steinke-Lange, V, Schmiegel, W, Vangala, D, Perne, C, Hüneburg, R, Redler, S, Büttner, R, Weitz, J, Pineda, M, Duenas, N, Vidal, J B, Moreira, L, Sánchez, A, Hovig, E, Nakken, S, Green, K, Lalloo, F, Hill, J, Crosbie, E, Mints, M, Goldberg, Y, Tjandra, D, Ten Broeke, S W, Kariv, R, Rosner, G, Advani, S H, Thomas, L, Shah, P, Shah, M, Neffa, F, Esperon, P, Pavicic, W, Torrezan, G T, Bassaneze, T, Martin, C A, Moslein, G & Moller, P 2023, ' Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment : a report from the prospective Lynch syndrome database ', EClinicalMedicine, vol. 58, 101909 . https://doi.org/10.1016/j.eclinm.2023.101909

مصطلحات موضوعية: kuolleisuus, perinnölliset taudit, Survival, MLH1, riskitekijät, General Medicine, MSH6, sukupuoli, MSH2, Cancer risk, Lynch syndrome, PMS2, syöpägeenit, syöpätaudit, Lynchin oireyhtymä, Mortality, Prospective study, ilmaantuvuus, ikä, henkiinjääminen, kohorttitutkimus

وصف الملف: application/pdf; ELETTRONICO; fulltext

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19f329812a94dc744ae88f2959a59615
https://vbn.aau.dk/ws/files/532406652/Dominguez_Valentin_et_al._2023_._Mortality_by_age_gene_and_gender_in_carriers_of_pathogenic_mismatch_repair_gene_variants_receiving_surveillance_for_early_cancer_diagnosis_and_treatment_a_report_from_the_prospective_Lynch.pdf

المؤلفون: Claudia Alejandra, Martin, Lourdes, Suárez Villasmil, Adela, Sembaj, Fabian, Gomez Balangione, Silvia, Zunino, Cecilia Del Carmen, Montes, Adriana, Borello, Andres, Del Castillo, Maximiliano, Zeballos, Norma Teresa, Rossi

المصدر: Revista de la Facultad de Ciencias Medicas (Cordoba, Argentina). 79(3)

مصطلحات موضوعية: BRCA2 Protein, Ovarian Neoplasms, Cross-Sectional Studies, BRCA1 Protein, Genes, BRCA2, Mutation, Argentina, Humans, Breast Neoplasms, Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::8efa82a8f08fa4d01102d141ffc33766
https://pubmed.ncbi.nlm.nih.gov/36149077

المؤلفون: Maria Nirvana Formiga, Joseph A. Pinto, Caroline U. Sa, Celia Aparecida Marques Pimenta, Julio Sanchez del Monte, Carlos A. Vaccaro, Mabel Bohorquez, Patricia Esperon, Florencia Spirandelli, Patricia Ashton-Prolla, Carmelo Caballero, Gutiérrez Angulo Melva, Maria del Carmen Castro-Mujica, Edite P. Oliveira, Norma Teresa Rossi, Sergio Chialina, Ivana Nascimento, Claudia Barletta-Carrillo, Larissa Souza Mario Bueno, Geth, Yesilda Balavarca, Jorge Padron, Edenir Inêz Palmero, Francisco López-Köstner, Sabrina Daniela da Silva, Nora Manoukian Forones, Juan Carlos Bazo-Alvarez, Florencia Neffa, Alcides Recalde Cañete, Mariela Torres Loarte, Pål Møller, Constantino Dominguez-Barrera, Mev Dominguez-Valentin, Pablo Kalfayan, John-Paul Plazzer, Jose Buleje, Kiyoko Abe-Sandes, Florencia C. Cardoso, Dirce Maria Carraro, Eivind Hovig, Patrik Wernhoff, Rodrigo Santa Cruz Guindalini, María Laura Gonzalez, Paola Montenegro Beltran, Marina Antelo, Angela R. Solano, Henrique de Campos Reis Galvão, Sonia Tereza dos Santos Nogueira, Samuel Aguiar Junior, Carlos Sarroca, Alberto Ignacio Herrando, Leonardo S. Lino-Silva, Carlos Mario Muñetón Peña, Tamara Alejandra Piñero, Erika Maria Monteiro Santos, Benedito Mauro Rossi, Mariano Golubicki, Yasser Sullcahuaman, Enrique Spirandelli, Geiner Jimenez, Karin Alvarez, Giovana Tardin Torrezan, Daniel Cisterna, Yenni Rodriguez, Richard Quispe, Ricardo Fujita, Claudia Martin, Della Valle Adriana, Renata Gondim Meira Velame de Azevedo, Lina Nuñez

المصدر: Repositorio Académico USMP
Universidad San Martín de Porres-USMP
USMP-Institucional
Universidad de San Martín de Porres
instacron:USMP
International Journal of Cancer
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid

مصطلحات موضوعية: Male, Cancer Research, Latin Americans, Colorectal cancer, Mini Review, colorectal cancer, Biology, MLH1, Risk Assessment, 03 medical and health sciences, 0302 clinical medicine, lynch syndrome, América Latina, Neoplasias colorrectales, parasitic diseases, medicine, PMS2, Humans, Early Detection of Cancer, Genetic testing, Neoplasias colorrectales hereditarias sin poliposis, medicine.diagnostic_test, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Lynch syndrome, Síndromes neoplásicos hereditarios, MSH6, Latin America, MutS Homolog 2 Protein, Oncology, MSH2, 030220 oncology & carcinogenesis, Practice Guidelines as Topic, Female, Guideline Adherence, MutL Protein Homolog 1, hereditary, Demography

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::877aeca091c95233becfe121cbeb957b
https://doi.org/10.1002/ijc.31920

المؤلفون: Patrik Wernhoff, Sergio Chialina, María Luisa Guevara Gil, María Laura Gonzalez, Luis José Palacios Fuenmayor, Constantino Dominguez-Barrera, Ana Protzel, Leonardo S. Lino-Silva, Michael Vallejo, Francisco López-Köstner, Karin Alvarez, Celia Aparecida Marques Pimenta, Julio Sanchez del Monte, Nadia Cambados Héritas, Carlos Mario Muñetón Peña, Jorge Andres Rugeles Mindiola, Elizabeth Lemos Silveira-Lucas, Eivind Hovig, Luisina Inés Bruno, Carlos Reyes-Silva, Alicia Cock-Rada, Florencia Neffa, Thais F Bonfim Palma, Richard Quispe, Alcides Recalde, Gabriela Jaramillo-Koupermann, Fabiana Alejandra Ferro, Norma Teresa Rossi, Mev Dominguez-Valentin, Florencia Spirandelli, Edenir Inêz Palmero, John-Paul Plazzer, Tirzah Braz Petta-Lajus, Sandra Patricia Bello Uyaban, Adriana Della Valle, Pål Møller, Ivana Nascimento, Marina Antelo, Jose Buleje, Kiyoko Abe-Sandes, Alejandra Mampel, Ana Rafaela de Souza Timoteo, Enrique Spirandelli, Julyann Pérez-Mayoral, Mariano Golubicki, Yasser Sullcahuaman, Alfonso Suárez, Mariela Torres, Henrique de Campos Reis Galvão, Carlos Sarroca, Magdalena Echeverry, Carlos Afanador Ayala, Claudia Martin, Guiliana Chávez, Jesús Arturo Hernández-Sandoval, Angélica Hernandez Guerrero, Geiner Jimenez, Yeni Rodriguez, Cladelis Rubio, Tamara Alejandra Piñero, Marcia Cruz-Correa, Pablo Kalfayan, Benedito Mauro Rossi, Florencia Petracchi, María de la Luz Ayala-Madrigal, Yesilda Balavarca, Juan Carlos Bazo-Alvarez, Carlos A. Vaccaro, Mabel Bohorquez, Milagros Dueñas, Nora Manoukian Forones, Claudio Benavides Yañez

المصدر: European journal of cancer (Oxford, England : 1990). 119

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Cancer Research, Latin Americans, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Surveys and Questionnaires, Medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, Registries, Genetic testing, medicine.diagnostic_test, business.industry, Middle Aged, South America, medicine.disease, Epithelial Cell Adhesion Molecule, Colorectal Neoplasms, Hereditary Nonpolyposis, Lynch syndrome, DNA-Binding Proteins, 030104 developmental biology, MutS Homolog 2 Protein, Oncology, 030220 oncology & carcinogenesis, Female, business, MutL Protein Homolog 1, Demography

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e288aad80099e1069fea7e6d4d5a63c6
https://pubmed.ncbi.nlm.nih.gov/31442815

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 Madrid

مصطلحات 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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db8010833347048c9dc625137680400a
https://hdl.handle.net/10642/7296