Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Alexandra Pickard"'
Autor:
Saskia C. Sanderson, Lauren Roberts, Cecilia Vindrola-Padros, Sarah L. Wynn, Monica Lakhanpaul, Celine Lewis, Angus Clarke, James Buchanan, Bettina Friedrich, Emma Clement, Melissa Hill, Jillian Hastings-Ward, Anneke M. Lucassen, Ruth Horn, Alexandra Pickard, Chris Patch
Publikováno v:
NIHR Open Research, Vol 1 (2022)
Background: A new nationally commissioned NHS England Genomic Medicine Service (GMS) was recently established to deliver genomic testing with equity of access for patients affected by rare diseases and cancer. The overarching aim of this research is
Externí odkaz:
https://doaj.org/article/74dd057649cd4b4692fbc10805cbd7c6
Autor:
Saskia C. Sanderson, Lauren Roberts, Cecilia Vindrola-Padros, Sarah L. Wynn, Monica Lakhanpaul, Celine Lewis, Angus Clarke, James Buchanan, Bettina Friedrich, Emma Clement, Melissa Hill, Jillian Hastings-Ward, Anneke M. Lucassen, Ruth Horn, Alexandra Pickard, Chris Patch
Publikováno v:
NIHR Open Research, Vol 1 (2021)
Background: A new nationally commissioned NHS England Genomic Medicine Service (GMS) was recently established to deliver genomic testing with equity of access for patients affected by rare diseases and cancer. The overarching aim of this research is
Externí odkaz:
https://doaj.org/article/c79370988e684cb59d6ce1bf20a1d55a
Autor:
Celine, Lewis, James, Buchannan, Angus, Clarke, Emma, Clement, Bettina, Friedrich, Jillian, Hastings-Ward, Melissa, Hill, Ruth, Horn, Anneke M, Lucassen, Chris, Patch, Alexandra, Pickard, Lauren, Roberts, Saskia C, Sanderson, Sarah L, Lewell, Cecilia, Vindrola-Padros, Monica, Lakhanpaul
Publikováno v:
NIHR open research
Background A new nationally commissioned NHS England Genomic Medicine Service (GMS) was recently established to deliver genomic testing with equity of access for patients affected by rare diseases and cancer. The overarching aim of this research is t
Autor:
Melissa Hill, Bettina Friedrich, Anneke Lucassen, Sarah L. Lewell, Lauren Roberts, Angus John Clarke, Ruth Horn, Celine Lewis, Cecilia Vindrola-Padros, Monica Lakhanpaul, Chris Patch, Emma Clement, Saskia C. Sanderson, Jillian Hastings-Ward, Alexandra Pickard, James Buchannan
Background: A new nationally commissioned NHS England Genomic Medicine Service (GMS) was recently established to deliver genomic testing with equity of access for patients affected by rare diseases and cancer. The overarching aim of this research is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fc447f3f6b37aca99dc811e4f674b8c