Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Gioconda Manassero-Morales"'
Autor:
Jeny Bazalar-Montoya, Mario Cornejo-Olivas, Milagros M. Duenas-Roque, Nelson Purizaca-Rosillo, Richard S. Rodriguez, Karina Milla-Neyra, Carlos A. De La Torre-Hernandez, Elison Sarapura-Castro, Carolina I. Galarreta Aima, Gioconda Manassero-Morales, Giulliana Chávez-Pasco, Luis Celis-García, Jorge E. La Serna-Infantes, Illumina Laboratory Services Bioinformatics, Software, Interpretation and Customer Support, Evgenii Chekalin, Erin Thorpe, Ryan J. Taft
Publikováno v:
npj Genomic Medicine, Vol 9, Iss 1, Pp 1-10 (2024)
Abstract There is limited access to molecular genetic testing in most low- and middle-income countries. The iHope program provides clinical genome sequencing (cGS) to underserved individuals with signs or symptoms of rare genetic diseases and limited
Externí odkaz:
https://doaj.org/article/53386bc0911340c4b23eb12d080b42fa
Autor:
Giulliana Chávez-Pasco, Jeny Bazalar-Montoya, Cecilia Bonilla Suarez, Krista Bluske, Samuel Strom, Alka Malhotra, Becky Milewski, Erin Thorpe, Ryan Taft, Gioconda Manassero-Morales
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101262- (2024)
Externí odkaz:
https://doaj.org/article/365afadaa8a94fe88ff2857264cbc533
Autor:
Jeny Bazalar-Montoya, Richard Rodriguez, Giulliana Chávez-Pasco, Peggy Martínez-Esteban, Revathi Rajkumar, Akanchha Kesari, Carolyn Brown, Erin Thorpe, Ryan Taft, Gioconda Manassero-Morales
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101306- (2024)
Externí odkaz:
https://doaj.org/article/ed917925916143929e44000368191b2d
Autor:
Erin Thorpe, Milagros Duenas-Roque, Mario Cornejo-Olivas, Jeny Bazalar-Montoya, Nelson Purizaca-Rosillo, Richard Rodriguez, Karina Milla-Neyra, Carlos De La Torre-Hernandez, Elison Sarapura-Castro, Carolina Galarreta Aima, Gioconda Manassero-Morales, Giulliana Chávez-Pasco, Luis Celis-García, Jorge La Serna, Ryan Taft
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101530- (2024)
Externí odkaz:
https://doaj.org/article/64256941fef24bb8a190dff98d515d0a
Autor:
Maria Colquicocha-Murillo, Janetliz Cucho-Jurado, Renee Mercedes Eyzaguirre-Zapata, Gioconda Manassero-Morales, Mariela del Carmen Moreno-Larrea, Katia Liliana Salas-Arbizu, Aimee Margarita Torres-Argandoña, Jesús Olga Vargas-Castro
Publikováno v:
Revista Médica Herediana, Vol 26, Iss 2, Pp 103-121 (2015)
Externí odkaz:
https://doaj.org/article/1f71743e8c7d44f18fa6173c5b98d158
Publikováno v:
Case Reports in Pediatrics, Vol 2016 (2016)
Introduction. The coexistence of Down and Turner syndromes due to double chromosome aneuploidy is very rare; it is even more rare to find the presence of a double monoclonal chromosomal abnormality. Objective. To report a unique case of double monocl
Externí odkaz:
https://doaj.org/article/3c60272c5d5c4cfab05792f91298915d
Autor:
Milagros M. Dueñas-Roque, Eduardo Acevedo-Vásquez, Cesar Sanchez, Hugo Abarca-Barriga, Alejandro Piscoya, Luis Jaramillo-Valverde, Pilar Mazzetti, Julio A. Poterico, Gioconda Manassero-Morales, Manuel F. Ugarte-Gil, Yasser Sullcahuaman-Allende, Ricardo Fujita, Kelly S. Levano, Heinner Guio, Mario Cornejo-Olivas, Juan Manuel Iglesias-Pedraz, Sandro Casavilca-Zambrano
Publikováno v:
Molecular Genetics & Genomic Medicine
Universidad San Ignacio de Loyola
Repositorio Institucional-USIL
USIL-Institucional
instacron:USIL
Repositorio Académico USMP
Universidad San Martín de Porres-USMP
USMP-Institucional
Universidad de San Martín de Porres
instacron:USMP
Universidad San Ignacio de Loyola
Repositorio Institucional-USIL
USIL-Institucional
instacron:USIL
Repositorio Académico USMP
Universidad San Martín de Porres-USMP
USMP-Institucional
Universidad de San Martín de Porres
instacron:USMP
Peru is a pluricultural and ethnically diverse country located in middle west of South America. It is the fourth largest country (1,285,216 km2) in area in South America, bordered in the north by Ecuador and Colombia, in the south by Chile, south eas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5075cec2d9f1a05b7c48681fb21450c1
http://europepmc.org/articles/PMC6305655
http://europepmc.org/articles/PMC6305655
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2016 (2016)
Case Reports in Pediatrics, Vol 2016 (2016)
Introduction. The coexistence of Down and Turner syndromes due to double chromosome aneuploidy is very rare; it is even more rare to find the presence of a double monoclonal chromosomal abnormality.Objective. To report a unique case of double monoclo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86b6e16fb24c7d5236cdc625787ccb30
https://doi.org/10.1155/2016/8760504
https://doi.org/10.1155/2016/8760504
Publikováno v:
Revista chilena de pediatría v.87 n.6 2016
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b19dca203a2320df7b2e8c7cdcbc2919
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062016000600014
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062016000600014
Autor:
Gioconda Manassero Morales
Publikováno v:
Revista de la Facultad de Medicina Humana; Vol 16 No 1 (2016): Revista de la Facultad de Medicina Humana
Revista de la Facultad de Medicina Humana; Vol. 16 Núm. 1 (2016): Revista de la Facultad de Medicina Humana
Revistas Universidad Ricardo Palma
Universidad Ricardo Palma
instacron:URP
Revista de la Facultad de Medicina Humana; Vol. 16 Núm. 1 (2016): Revista de la Facultad de Medicina Humana
Revistas Universidad Ricardo Palma
Universidad Ricardo Palma
instacron:URP
El síndrome Down es la causa genética más frecuente de retardo mental en los seres humanos. Uno de cada 700 – 800 niños nace con esta patología. En nuestro país no existen datos epidemiológicos que reporten su incidencia ni su prevalencia. D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1f7bf52e25ca97c3d9d9e6a58a1c1c6
https://doi.org/10.25176/rfmh.v16.n1.338
https://doi.org/10.25176/rfmh.v16.n1.338