학술논문
Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing
Document Type
Article
Author
Hocking, L.J.; Miedzybrodzka, Z.; Andrews, C.; Baty, D.; Berg, J.; Armstrong, C.; Clark, C.; O’Sullivan, D.; Ansari, M.; Diamond, A.; Lampe, A.; Moore, D.J.; Fletcher, E.; Lam, W.; Porteous, M.; Bradley, T.; Doherty, J.; McGowan, R.; Purvis, A.; Westwood, P.; Williams, N.; Santoyo-Lopez, J.; Abbott, M.; Aitman, T.J.; Dean, J.; Foley, P.; Robertson, L.; Ross, A.; Williamson, K.; Aitman, T.J.; Humphrey, W.I.; Meynert, A.; Semple, C.A.; Biankin, A.V.; Cooke, S.L.; Martin, S.; Nourse, C.; Murphy, F.; Barr, K.; Williams, N.; Bradshaw, N.; Davidson, R.; Gardiner, C.; Gorrie, J.; Hamilton, M.; Joss, S.; Kinning, E.; Longman, C.; Martin, N.; McGowan, R.; Paterson, J.; Pilz, D.; Snadden, L.; Tobias, E.; Wedderburn, S.; Whiteford, M.; Berg, J.; Goudie, D.; McWilliam, C.; Fitzpatrick, D.; Jackson, A.; Hague, R.
Source
In: European Journal of Human Genetics . (European Journal of Human Genetics, February 2023, 31(2):231-238)
Subject
Language
English
ISSN
14765438
10184813
10184813