Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Idarmis Jiménez Torres"'
Autor:
César Paz‐y‐Miño, Verónica Yumiceba, Germania Moreta, Rosario Paredes, Mónica Ruiz, Ligia Ocampo, Arianne Llamos Paneque, Catalina Ochoa Pérez, Juan Carlos Ruiz‐Cabezas, Jenny Álvarez Vidal, Idarmis Jiménez Torres, Ramón Vargas‐Vera, Fernando Cruz, Víctor Hugo Guapi N, Martha Montalván, Sara Meneses Álvarez, Maribel Garzón Castro, Elizabeth Lamar Segura, María Augusta Recalde Báez, María Elena Naranjo, Nina Tambaco Jijón, María Sinche, Pedro Licuy, Ramiro Burgos, Fabián Porras‐Borja, Gabriela Echeverría‐Garcés, Andy Pérez‐Villa, Isaac Armendáriz‐Castillo, Jennyfer M. García‐Cárdenas, Santiago Guerrero, Patricia Guevara‐Ramírez, Andrés López‐Cortés, Ana Karina Zambrano, Paola E. Leone
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 2, Pp n/a-n/a (2020)
Abstract Background Detection of chromosomal abnormalities is crucial in various medical areas; to diagnose birth defects, genetic disorders, and infertility, among other complex phenotypes, in individuals across a wide range of ages. Hence, the pres
Externí odkaz:
https://doaj.org/article/fa712656beb6407583de34aee63b8326
Autor:
Andy Pérez-Villa, Gabriela Echeverría-Garcés, Arianne Llamos Paneque, María Sinche, Catalina Ochoa Pérez, Germania Moreta, Pedro Licuy, Patricia Guevara-Ramírez, Ramiro Burgos, Nina Jacinta Tambaco Jijón, Ramón Vargas‐Vera, Juan Carlos Ruiz-Cabezas, Jennyfer M. García-Cárdenas, César Paz-y-Miño, Verónica Yumiceba, Elizabeth Lamar Segura, Isaac Armendáriz-Castillo, Santiago Guerrero, Martha Montalván, Ana Karina Zambrano, Andrés López-Cortés, Fabián Porras-Borja, Jenny Álvarez Vidal, Fernando Cruz, Víctor Hugo Guapi N, María Elena Naranjo, Mónica Ruiz, Maribel de los Ángeles Garzón Castro, Rosario Paredes, Idarmis Jiménez Torres, María Augusta Recalde Báez, Paola E. Leone, Sara Meneses Álvarez, Ligia Ocampo
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 2, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 2, Pp n/a-n/a (2020)
Background Detection of chromosomal abnormalities is crucial in various medical areas; to diagnose birth defects, genetic disorders, and infertility, among other complex phenotypes, in individuals across a wide range of ages. Hence, the present study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5204d1d256074c28a639e9c8bbb209ac
https://pubmed.ncbi.nlm.nih.gov/31830383
https://pubmed.ncbi.nlm.nih.gov/31830383