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A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype. [electronic resource] by
- Hergersberg, M
- Balakrishnan, J
- Bettecken, T
- Chevalier-Porst, F
- Brägger, C
- Burger, R
- Einschenk, I
- Liechti-Gallati, S
- Morris, M
- Schorderet, D
- Thonney, F
- Moser, H
- Malik, N
Producer: 19970908
In:
Human genetics vol. 100
Availability: No items available.
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