Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Genetic mapping arrays"'
Autor:
Paola E. Leone, Verónica Yumiceba, Ariana Jijón-Vergara, Andy Pérez-Villa, Isaac Armendáriz-Castillo, Jennyfer M. García-Cárdenas, Santiago Guerrero, Patricia Guevara-Ramírez, Andrés López-Cortés, Ana K. Zambrano, Jesús M. Hernández-Rivas, Juan Luis García, César Paz-y-Miño
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-9 (2020)
Abstract Background Turner syndrome is a genetic disorder that affects women. It is caused by an absent or incomplete X chromosome, which can be presented in mosaicism or not. There are 12 cases of Turner syndrome patients who present structural alte
Externí odkaz:
https://doaj.org/article/2c3597f4f75d4d4f90fb70e2316006d5
Autor:
Leone, Paola E.1 (AUTHOR) paola.leone@ute.edu.ec, Yumiceba, Verónica1 (AUTHOR), Jijón-Vergara, Ariana1 (AUTHOR), Pérez-Villa, Andy1 (AUTHOR), Armendáriz-Castillo, Isaac1 (AUTHOR), García-Cárdenas, Jennyfer M.1 (AUTHOR), Guerrero, Santiago1 (AUTHOR), Guevara-Ramírez, Patricia1 (AUTHOR), López-Cortés, Andrés1 (AUTHOR), Zambrano, Ana K.1 (AUTHOR), Hernández-Rivas, Jesús M.2,3 (AUTHOR), García, Juan Luis3,4 (AUTHOR), Paz-y-Miño, César1 (AUTHOR) cesar.pazymino@ute.edu.ec
Publikováno v:
Molecular Cytogenetics (17558166). 11/13/2020, Vol. 13 Issue 1, p1-9. 9p.
Autor:
Andy Pérez-Villa, Verónica Yumiceba, Ana Karina Zambrano, Jennyfer M. García-Cárdenas, Patricia Guevara-Ramírez, Andrés López-Cortés, Paola E. Leone, Santiago Guerrero, Jesús M. Hernández-Rivas, Ariana Jijón-Vergara, Isaac Armendáriz-Castillo, Juan Luis García, César Paz-y-Miño
Publikováno v:
GREDOS. Repositorio Institucional de la Universidad de Salamanca
instname
GREDOS: Repositorio Institucional de la Universidad de Salamanca
Universidad de Salamanca (USAL)
Molecular Cytogenetics
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-9 (2020)
instname
GREDOS: Repositorio Institucional de la Universidad de Salamanca
Universidad de Salamanca (USAL)
Molecular Cytogenetics
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-9 (2020)
Background Turner syndrome is a genetic disorder that affects women. It is caused by an absent or incomplete X chromosome, which can be presented in mosaicism or not. There are 12 cases of Turner syndrome patients who present structural alterations i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::354e2eeb2ab64f73b69b05afd99d9a8e
http://hdl.handle.net/10366/145408
http://hdl.handle.net/10366/145408
Autor:
Paz-y-Miño, César1 (AUTHOR) genetica_medica@cesarpazymino.com, Vargas-Vera, Ramón Miguel2 (AUTHOR) dr.ramonvargasvera@hotmail.com, Placencia-Ibadango, Martha Verónica3 (AUTHOR), Vargas-Silva, Kalid Stefano4 (AUTHOR), García-Hernández, Juan Luis5 (AUTHOR), Balarezo-Díaz, Thalía6 (AUTHOR), Leone, Paola E.7 (AUTHOR)
Publikováno v:
Molecular Cytogenetics (17558166). 10/31/2024, Vol. 17 Issue 1, p1-9. 9p.
Autor:
Paz‐y‐Miño, César1 (AUTHOR) cesar.pazymino@ute.edu.ec, Yumiceba, Verónica1 (AUTHOR), Moreta, Germania2 (AUTHOR), Paredes, Rosario2 (AUTHOR), Ruiz, Mónica3 (AUTHOR), Ocampo, Ligia4 (AUTHOR), Llamos Paneque, Arianne2 (AUTHOR), Ochoa Pérez, Catalina5 (AUTHOR), Ruiz‐Cabezas, Juan Carlos6,7 (AUTHOR), Álvarez Vidal, Jenny8 (AUTHOR), Jiménez Torres, Idarmis9 (AUTHOR), Vargas‐Vera, Ramón10 (AUTHOR), Cruz, Fernando11 (AUTHOR), Guapi N, Víctor Hugo12 (AUTHOR), Montalván, Martha13 (AUTHOR), Meneses Álvarez, Sara14 (AUTHOR), Garzón Castro, Maribel2 (AUTHOR), Lamar Segura, Elizabeth2 (AUTHOR), Recalde Báez, María Augusta2 (AUTHOR), Naranjo, María Elena2 (AUTHOR)
Publikováno v:
Molecular Genetics & Genomic Medicine. Feb2020, Vol. 8 Issue 2, pN.PAG-N.PAG. 1p.