Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Taylor Cain"'
Autor:
Mohammad Eldomery, Patrick Blackburn, Taylor Cain, Victor Pastor Loyola, David Wheeler, Lu Wang, Jeffery M. Klco, Jamie Maciaszek
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 100940- (2024)
Externí odkaz:
https://doaj.org/article/aa1ba1b2efd143c0ae61a04aa034733d
Autor:
Xubin Li, Qing Deng, Jared Henderson, Grace Watson, Laurel Deaton, Taylor Cain, Luis Fayad, Swaminathan Padmanabhan Iyer, Fredrick B. Hagemeister, Loretta J. Nastoupil, Nathan H. Fowler, Jason Westin, Raphael Steiner, Ranjit Nair, Sairah Ahmed, Gheath Alatrash, Sattva S. Neelapu, Paolo Strati, Michael R Green
Publikováno v:
Blood. 140:4502-4503
Autor:
Taylor Cain
Publikováno v:
Journal of Urban Affairs. 42:1222-1241
The migration patterns of middle-class families in urban landscapes has been a point of discussion in studies of gentrification since the 1980s; however, most studies focus on the movements of fami...
Autor:
Paolo Strati, Xubin Li, Qing Deng, Mario Luiz Marques-Piubelli, Jared Henderson, Grace Balada, Laurel Deaton, Taylor Cain, Haopeng Yang, Vida Ravanmehr, Luis E. Fayad, Swaminathan Iyer, Loretta J. Nastoupil, Fredrick B. Hagemeister, Nathan H. Fowler, Jason R. Westin, Raphael E. Steiner, Ranjit Nair, Christopher R. Flowers, Linghua Wang, Sairah Ahmed, Gheath Al-Atrash, Francisco Vega, Sattva S. Neelapu, Michael Green
Publikováno v:
SSRN Electronic Journal.
Autor:
Amal Yussuf, Rachel McFarland, Patrick Reineke, Stephanie Gutierrez, Jonathan Pepper, Holly LaDuca, Taylor Cain, Kirsten Blanco, Carolyn Horton, Nadia Ho, Jill S. Dolinsky
Publikováno v:
JCO Clinical Cancer Informatics. :1-11
Purpose Clinical history data reported on test requisition forms (TRFs) for hereditary cancer multigene panel testing (MGPT) are routinely used by genetic testing laboratories. More recently, publications have incorporated TRF-based clinical data int
Autor:
Dima El-Khechen, Kelly D. Farwell Hagman, Benjamin Feldmann, Taylor Cain, Kirsten Blanco, Julie Stefka, Meghan C. Towne
Publikováno v:
Journal of genetic counselingREFERENCES. 31(3)
Access to genetic testing, namely, diagnostic exome sequencing (DES), has significantly improved, subsequently increasing the likelihood of discovering incidental findings, such as misattributed relationships and specifically misattributed parentage
Publikováno v:
ECS Meeting Abstracts. :574-574
Autor:
Taylor Cain
Publikováno v:
City & Community. 16:232-234
Autor:
Kirsten Blanco, Layla Shahmirzadi Mowlavi, Kelly D. Farwell Hagman, Gerald Vockley, Lina Gonzalez, Emily M. Mayerhofer, Taylor Cain, Zöe Powis, Sha Tang, Virginia Speare, Marilyn Tsang, David Tilstra, Jesse M. Hunter, Timothy Vedder
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 20(11)
Neonatal patients are particularly appropriate for utilization of diagnostic exome sequencing (DES), as many Mendelian diseases are known to present in this period of life but often with complex, heterogeneous features. We attempted to determine the
Autor:
Taylor Cain
Publikováno v:
Agriculture and Human Values. 31:689-690
An insightful and stimulating read, this edited volume by Finnis, an associate professor in the Department of Sociology and Anthropology at the University of Guelph, explores the intellectual trajectory of marginality through contemporary food system