Author/Creator: Ballmann, M - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Ballmann, M

1. Diversity of the basic defect of homozygous CFTR mutation genotypes in humans. Issue 1 (4th January 2008)

Authors:: Stanke, F; Ballmann, M; Bronsveld, I; Dörk, T; Gallati, S; Laabs, U; Derichs, N; Ritzka, M; Posselt, H-G; Harms, H K; Griese, M; Blau, H; Mastella, G; Bijman, J; Veeze, H; Tümmler, B
Journal:: Journal of medical genetics
Issue:: Volume 45:Issue 1(2008)
Page Start:: 47
Record Type:: Journal Article
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2. Transient correction of the basic defect in sweat glands in an individual with cystic fibrosis carrying the complex CFTR allele F508del-R553Q. Issue 2 (28th January 2009)

Authors:: Tümmler, B; Stanke, F; Bronsveld, I; Veeze, H; Ballmann, M
Journal:: Thorax
Issue:: Volume 64:Issue 2(2009)
Page Start:: 179
Record Type:: Journal Article
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