Association of less common cystic fibrosis mutations with a mild phenotype.

Author:

Curtis A,Nelson R,Porteous M,Burn J,Bhattacharya S S

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference11 articles.

1. Identification of cystic fibrosis gene: cloning and characterisation of complementary DNA;Riordan, JR, Rommens; JM, Kerem; B.S.;Science,1989

2. Identification of the cystic fibrosis gene: genetic analysis;Kerem, B.S.; Rommens, J.M.; Buchanan, J.A.;Science,1989

3. Gradient of distribution in Europe of the major CF mutation and its associated haplotype. Hum Genet;on CF Genetics, European Working Group

4. The haplotype distribution of the delta F508 mutation in cystic fibrosis families in Scotland;McIntosh, I.; Curtis, A.; Lorenzo, M.L.;Hum Genet,1990

5. Tracing the mutations in cystic fibrosis by means of closely linked DNA markers;Tsui, L.C.;Am J Hum Genet,1989

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