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Experiences from whole genome sequencing in diagnostics - broad in silico panels and introducing structural variant detection
- Nilsson, D (author)
- Robinson, KL (author)
- Malmgren, H (author)
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- Karlsson, M (author)
- Gustavsson, P (author)
- Hammarsjo, A (author)
- Grigelioniene, G (author)
- Arce, MP (author)
- Tham, E (author)
- Pigg, MH (author)
- Nordgren, A (author)
- Jorholt, J (author)
- Kvarnung, M (author)
- Lieden, A (author)
- Lundin, J (author)
- Eisfeldt, J (author)
- Lindstrand, A (author)
- Wirta, V (author)
- Nordenskjold, M (author)
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- (creator_code:org_t)
- 2018
- 2018
- English.
- In: EUROPEAN JOURNAL OF HUMAN GENETICS. - 1018-4813. ; 26, s. 677-677
- Conference paper (other academic/artistic)
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- vet (subject category)
- kon (subject category)
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- EUROPEAN JOURNAL OF HUMAN GENETICS (Search for host publication in LIBRIS)
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- Nilsson, D
- Robinson, KL
- Malmgren, H
- Karlsson, M
- Gustavsson, P
- Hammarsjo, A
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- Grigelioniene, G
- Arce, MP
- Tham, E
- Pigg, MH
- Anderlid, B
- Nordgren, A
- Jorholt, J
- Kvarnung, M
- Sejersen, T
- Lieden, A
- Lundin, J
- Eisfeldt, J
- Lindstrand, A
- Wirta, V
- Nordenskjold, M
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- Karolinska Institutet
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