Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sally Ann Rodríguez"'
Autor:
Ashok Agarwal, Signe Altmäe, Ester Anton, Rosa Roy Barcelona, Lluís Bassas, Davina Bonte, José P. Carrascosa, Petra De Sutter, Aysenur Ersoy, Francisco J. Esteban, José Luís Fernández, A.F. Fernández, M.F. Fraga, Iria González-Vasconcellos, Jaime Gosálvez, Ramesh Reddy Guggilla, Sezgin Gunes, Samir Hamamah, Delphine Haouzi, Björn Heindryckx, Ralf Henkel, William V. Holt, José A. Horcajadas, Meritxell Jodar, Ahmet Kablan, Neha Kumar, Sara Larriba, Giulia Mariani, Swati Mishra, Juan M. Moreno-Moya, Santiago Munne, Sergio Oehninger, José Bellver Pradas, Anaís García Rodríguez, Sally Ann Rodríguez, Sarthak Sawarkar, Panagiotis Stamatiadis, Jasin Taelman, R.G. Urdinguio, Margot Van der Jeught, Eva Vargas, Xavier Vendrell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8153fd127c90773e2d6623cc94f7ae9
https://doi.org/10.1016/b978-0-12-812571-7.09989-5
https://doi.org/10.1016/b978-0-12-812571-7.09989-5
Autor:
Sally Ann Rodríguez, N. Kumar
It is estimated that approximately 80% of children born with a genetic condition have no family history of that disease. This is often due to the fact that many genetic conditions follow a recessive inheritance pattern, and thus, carriers are general
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4857dc0c2ff15e5e84e122d6c674621
https://doi.org/10.1016/b978-0-12-812571-7.00005-8
https://doi.org/10.1016/b978-0-12-812571-7.00005-8
Autor:
Sally Ann Rodríguez, Debra L. Roter, Lori H. Erby, Carlos Castillo-Salgado, Gillian W. Hooker
Publikováno v:
Health Psychology. 34:120-129
OBJECTIVE Literacy deficits and underutilization of medical services have been linked to health disparities among minorities, and this appears especially relevant for the Latino population. Given the increasing importance of genetics, assessment of g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21aafa450c36794de67b0ef23c5057a0
https://doi.org/10.1037/hea0000162
https://doi.org/10.1037/hea0000162
Autor:
Jamie Grifo, Shahin Ghadir, Serena H. Chen, Sally Ann Rodríguez, Sonya Elango, A. Manoharan, A. Hershlag, Sara L. Bristow, David Hoffman, S. Yarnall, N. Kumar, R. Shraga, Oscar Puig, Mohammad Niknazar, Rita Vassena
Publikováno v:
BMC Genetics
BMC Genetics, Vol 18, Iss 1, Pp 1-9 (2017)
BMC Genetics, Vol 18, Iss 1, Pp 1-9 (2017)
BackgroundCurrent professional society guidelines recommend genetic carrier screening be offered on the basis of ethnicity, or when using expanded carrier screening panels, they recommend to compute residual risk based on ethnicity. We investigated t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8208b57f496d36c069c06c5a7fd403e
Publikováno v:
American Journal of Obstetrics and Gynecology. 216:S146-S147
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::991eda47c775ff9e1478d803d5f35b8a
https://doi.org/10.1016/j.ajog.2016.11.138
https://doi.org/10.1016/j.ajog.2016.11.138
Autor:
Nicholas De Veaux, R. Prates, Charlotte Rivera-Garcia, Sally Ann Rodríguez, Alexander Bisignano, N. Kumar, S. Yarnall, Sara L. Bristow, Santiago Munné, Bo Chu
Publikováno v:
Genetics in Medicine.
Technological advances now allow for multiplex platforms to simultaneously test many genetic conditions. Typically, such platforms are validated by assaying samples with known genotypes and/or phenotypes and/or with synthetic plasmids; however, these
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af0c8fc0ed5114de904ba9e0194ca843
https://doi.org/10.1038/gim.2015.101
https://doi.org/10.1038/gim.2015.101
Autor:
Roman Shraga, Sarah Yarnall, Sonya Elango, Arun Manoharan, Sally Ann Rodriguez, Sara L. Bristow, Neha Kumar, Mohammad Niknazar, David Hoffman, Shahin Ghadir, Rita Vassena, Serena H. Chen, Avner Hershlag, Jamie Grifo, Oscar Puig
Publikováno v:
BMC Genetics, Vol 18, Iss 1, Pp 1-9 (2017)
Abstract Background Current professional society guidelines recommend genetic carrier screening be offered on the basis of ethnicity, or when using expanded carrier screening panels, they recommend to compute residual risk based on ethnicity. We inve
Externí odkaz:
https://doaj.org/article/3b3d6e6b49e743de86941d8df101717f