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[The utility of whole genome sequencing in rare disease diagnostics]
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- Johansson Soller, M (author)
- Karolinska Institutet
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- Nordgren, A (author)
- Karolinska Institutet
- Ehrencrona, H (author)
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- Lovmar, L (author)
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- (creator_code:org_t)
- 2021
- 2021
- English.
- In: Lakartidningen. - 1652-7518. ; 118
- Journal article (peer-reviewed)
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- Ehrencrona, H
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