Similar articles for PMID: 7682984

Year	Number of Results
1990	2
1991	12
1992	37
1993	21
1994	30
1995	20
1996	1
1997	1
1998	1
2000	1
2024	0

1

A novel mutation in exon 3 of the CFTR gene.

Guillermit H, Jéhanne M, Quéré I, Audrézet MP, Mercier B, Férec C. Guillermit H, et al. Hum Genet. 1993 Apr;91(3):233-5. doi: 10.1007/BF00218262. Hum Genet. 1993. PMID: 7682984

2

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.

3

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

4

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

5

Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Zielenski J, Bozon D, Kerem B, Markiewicz D, Durie P, Rommens JM, Tsui LC. Zielenski J, et al. Genomics. 1991 May;10(1):229-35. doi: 10.1016/0888-7543(91)90504-8. Genomics. 1991. PMID: 1710599

6

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

7

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

8

Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctions.

Fanen P, Ghanem N, Vidaud M, Besmond C, Martin J, Costes B, Plassa F, Goossens M. Fanen P, et al. Genomics. 1992 Jul;13(3):770-6. doi: 10.1016/0888-7543(92)90152-i. Genomics. 1992. PMID: 1379210

9

Frequency of the delta F508 and exon 11 mutations in Norwegian cystic fibrosis patients.

Eiklid K, Tranebjaerg L, Eiken HG, Pedersen JC, Michalsen H, Fluge G, Schwartz M, Nilsen BR, Bolle R, Skyberg D, et al. Eiklid K, et al. Clin Genet. 1993 Jul;44(1):12-4. doi: 10.1111/j.1399-0004.1993.tb03834.x. Clin Genet. 1993. PMID: 7691448

10

Homozygosity for a novel missense mutation (I175V) in exon 5 of the CFTR gene in a family of Armenian descent.

Romey MC, Desgeorges M, Malzac P, Sarles J, Demaille J, Claustres M. Romey MC, et al. Hum Mol Genet. 1994 Apr;3(4):661-2. doi: 10.1093/hmg/3.4.661. Hum Mol Genet. 1994. PMID: 7520799 No abstract available.

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