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Stanke, F.; Ballmann, M.; Bronsveld, I.; Dörk, T.; Gallati, S.; Laabs, U.; Derichs, N.; Ritzka, M.; Posselt, H.-G.; Harms, H. K.; Griese, Matthias; Blau, H.; Mastella, G.; Bijman, J.; Veeze, V.; Tümmler, B. (2008): Diversity of the basic defect of homozygous CFTR mutation genotypes in humans. In: Journal of Medical Genetics, Vol. 45, No. 1: pp. 47-54 [PDF, 248kB]