Similar articles for PMID: 8097485

Year	Number of Results
1951	1
1990	10
1991	14
1992	21
1993	14
1994	12
1995	10
1996	2
1997	5
1998	1
1999	1
2000	1
2001	1
2005	1
2006	1
2014	1
2024	0

1

Analysis of 160 CF chromosomes: detection of a novel mutation in exon 20.

Dorval I, Odent S, Jezequel P, Journel H, Chauvel B, Dabadie A, Roussey M, Le Gall JY, Le Marec B, David V, et al. Dorval I, et al. Hum Genet. 1993 Apr;91(3):254-6. doi: 10.1007/BF00218266. Hum Genet. 1993. PMID: 8097485

2

Molecular and clinical findings in Austrian cystic fibrosis patients with mutations in exon 11 of the CFTR gene.

Greil I, Wagner K, Eber E, Zach M, Rosenkranz W. Greil I, et al. Wien Klin Wochenschr. 1995;107(15):464-9. Wien Klin Wochenschr. 1995. PMID: 7545856

3

Screening for non-delta F508 mutations in five exons of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Italy.

Devoto M, Ronchetto P, Fanen P, Orriols JJ, Romeo G, Goossens M, Ferrari M, Magnani C, Seia M, Cremonesi L. Devoto M, et al. Am J Hum Genet. 1991 Jun;48(6):1127-32. Am J Hum Genet. 1991. PMID: 1709778 Free PMC article.

4

Three point mutations in the CFTR gene in French cystic fibrosis patients: identification by denaturing gradient gel electrophoresis.

Vidaud M, Fanen P, Martin J, Ghanem N, Nicolas S, Goossens M. Vidaud M, et al. Hum Genet. 1990 Sep;85(4):446-9. doi: 10.1007/BF02428305. Hum Genet. 1990. PMID: 2210768

5

Identification of 12 novel mutations in the CFTR gene.

Audrézet MP, Mercier B, Guillermit H, Quéré I, Verlingue C, Rault G, Férec C. Audrézet MP, et al. Hum Mol Genet. 1993 Jan;2(1):51-4. doi: 10.1093/hmg/2.1.51. Hum Mol Genet. 1993. PMID: 7683952

6

Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families.

Dörk T, Neumann T, Wulbrand U, Wulf B, Kälin N, Maass G, Krawczak M, Guillermit H, Ferec C, Horn G, et al. Dörk T, et al. Hum Genet. 1992 Feb;88(4):417-25. doi: 10.1007/BF00215676. Hum Genet. 1992. PMID: 1371263

7

Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene.

Dörk T, Wulbrand U, Richter T, Neumann T, Wolfes H, Wulf B, Maass G, Tümmler B. Dörk T, et al. Hum Genet. 1991 Aug;87(4):441-6. doi: 10.1007/BF00197165. Hum Genet. 1991. PMID: 1715308

8

Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis.

Sereth H, Shoshani T, Bashan N, Kerem BS. Sereth H, et al. Hum Genet. 1993 Oct 1;92(3):289-95. doi: 10.1007/BF00244474. Hum Genet. 1993. PMID: 7691712

9

Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutations.

Dörk T, Fislage R, Neumann T, Wulf B, Tümmler B. Dörk T, et al. Hum Genet. 1994 Jan;93(1):67-73. doi: 10.1007/BF00218916. Hum Genet. 1994. PMID: 7505767

10

Mutation characterization of CFTR gene in 206 Northern Irish CF families: thirty mutations, including two novel, account for approximately 94% of CF chromosomes.

Hughes DJ, Hill AJ, Macek M Jr, Redmond AO, Nevin NC, Graham CA. Hughes DJ, et al. Hum Mutat. 1996;8(4):340-7. doi: 10.1002/(SICI)1098-1004(1996)8:4<340::AID-HUMU7>3.0.CO;2-B. Hum Mutat. 1996. PMID: 8956039

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