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- Nilsson, D (author)
Experiences from whole genome sequencing in diagnostics - broad in silico panels and introducing structural variant detection
- Article/chapterEnglish2018
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- 2018
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- LIBRIS-ID:oai:prod.swepub.kib.ki.se:142078921
- http://kipublications.ki.se/Default.aspx?queryparsed=id:142078921URI
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- Language:English
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- Robinson, KL (author)
- Malmgren, H (author)
- Karlsson, M (author)
- Gustavsson, P (author)
- Hammarsjo, A (author)
- Grigelioniene, G (author)
- Arce, MP (author)
- Tham, E (author)
- Pigg, MH (author)
- Anderlid, BKarolinska Institutet (author)
- Nordgren, A (author)
- Jorholt, J (author)
- Kvarnung, M (author)
- Sejersen, TKarolinska Institutet (author)
- Lieden, A (author)
- Lundin, J (author)
- Eisfeldt, J (author)
- Lindstrand, A (author)
- Wirta, V (author)
- Nordenskjold, M (author)
- Karolinska Institutet (creator_code:org_t)
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- In:EUROPEAN JOURNAL OF HUMAN GENETICS26, s. 677-6771018-4813
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