Multi‐institutional experience of genetic diagnosis in Ecuador: National registry of chromosome alterations and polymorphisms

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 wants to contribute to the knowledge of type and...

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Detalles Bibliográficos
Autores principales: Paz‐y‐Miño, César, Yumiceba, Verónica, Moreta, Germania, Paredes, Rosario, Ruiz, Mónica, Ocampo, Ligia, Llamos Paneque, Arianne, Ochoa Pérez, Catalina, Ruiz‐Cabezas, Juan Carlos, Álvarez Vidal, Jenny, Jiménez Torres, Idarmis, Vargas‐Vera, Ramón, Cruz, Fernando, Guapi N, Víctor Hugo, Montalván, Martha, Meneses Álvarez, Sara, Garzón Castro, Maribel, Lamar Segura, Elizabeth, Recalde Báez, María Augusta, Naranjo, María Elena, Tambaco Jijón, Nina, Sinche, María, Licuy, Pedro, Burgos, Ramiro, Porras‐Borja, Fabián, Echeverría‐Garcés, Gabriela, Pérez‐Villa, Andy, Armendáriz‐Castillo, Isaac, García‐Cárdenas, Jennyfer M., Guerrero, Santiago, Guevara‐Ramírez, Patricia, López‐Cortés, Andrés, Zambrano, Ana Karina, Leone, Paola E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005643/
https://www.ncbi.nlm.nih.gov/pubmed/31830383
http://dx.doi.org/10.1002/mgg3.1087

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005643/
https://www.ncbi.nlm.nih.gov/pubmed/31830383
http://dx.doi.org/10.1002/mgg3.1087

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