Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jessica Tyson"'
Publikováno v:
Frontiers in Environmental Science, Vol 8 (2020)
In order for land managers and policy makers to manage excessive soil phosphorus (P) concentrations and reduce the risk of this particular source of P from impacting water bodies, models of soil P decline under various scenarios are needed. We modell
Externí odkaz:
https://doaj.org/article/6f7b2e7a5a8e4669befa53a333b121c2
Publikováno v:
Frontiers in Environmental Science, Vol 8 (2020)
In order for land managers and policy makers to manage excessive soil phosphorus (P) concentrations and reduce the risk of this particular source of P from impacting water bodies, models of soil P decline under various scenarios are needed. We modell
Autor:
Frank J. Probst, Peter Hedera, Maria Grazia Pomponi, Julie A. Douglas, Giovanni Neri, Jessica Tyson, Donna M. Martin, Elizabeth M. Petty, Anthony M. Sclafani
Publikováno v:
American Journal of Medical Genetics. :209-212
Frank J. Probst, Peter Hedera, Anthony M. Sclafani, Maria Grazia Pomponi, Giovanni Neri, Jessica Tyson, Julie A. Douglas, Elizabeth M. Petty, and Donna M. Martin Department of Pediatrics, Cornell University Medical Center, New York, New York Departme
Autor:
Jessica Tyson
Publikováno v:
Pennsylvania Legacies. 17:32
Autor:
Jessica Tyson
Publikováno v:
Pennsylvania Legacies. 17:32
Autor:
Bjørn Aslaksen, J F Taylor, Ole Lund, Maria Bitner-Glindzicz, Shomi S. Bhattacharya, Jessica Tyson, Christopher Wren, Svein Jan Sørland, Sue Bellman, Marcus E. Pembrey, Lisbeth Tranebjærg, Jørn Bathen, Sue Malcolm
Publikováno v:
Human molecular genetics. 6(12)
The Jervell and Lange-Nielsen syndrome (JLNS) comprises profound congenital sensorineural deafness associated with syncopal episodes. These are caused by ventricular arrhythmias secondary to abnormal repolarisation, manifested by a prolonged QT inter
Autor:
Elizabeth M. Petty, Julie A. Douglas, Anthony M. Sclafani, Giovanni Neri, Jessica Tyson, Donna M. Martin, Maria Grazia Pomponi, Peter Hedera, Frank J. Probst
Publikováno v:
American Journal of Medical Genetics Part A. :347-347