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Three common CFTR mutations should be included in a neonatal screening programme for cystic fibrosis in Sweden
- Schaedel, C (author)
-
- Hjelte, L (author)
- Karolinska Institutet
-
- de Monestrol, I (author)
- Karolinska Institutet
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- Kornfalt, R (author)
- Holmberg, L (author)
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- (creator_code:org_t)
- 2001-12-24
- 1999
- English.
- In: Clinical genetics. - : Wiley. - 0009-9163. ; 56, s. 318-
- Journal article (peer-reviewed)
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- Schaedel, C
- Hjelte, L
- de Monestrol, I
- Johannesson, M
- Kollberg, H
- Kornfalt, R
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- Holmberg, L
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- Clinical genetic ...
- Clin Genet
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- Uppsala University
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