207 related articles for article (PubMed ID: 1370807)
1. Single-strand conformation polymorphism (SSCP) analysis of exon 11 of the CFTR gene reliably detects more than one third of non-delta F508 mutations in German cystic fibrosis patients.
Plieth J; Rininsland F; Schlösser M; Cooper DN; Reiss J
Hum Genet; 1992 Jan; 88(3):283-7. PubMed ID: 1370807
[TBL] [Abstract][Full Text] [Related]
2. 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
Hum Genet; 1991 Aug; 87(4):441-6. PubMed ID: 1715308
[TBL] [Abstract][Full Text] [Related]
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
Am J Hum Genet; 1991 Jun; 48(6):1127-32. PubMed ID: 1709778
[TBL] [Abstract][Full Text] [Related]
4. A novel CFTR mutation, 4035delA, detected by non-radioactive SSCP analysis.
Reiss J; Lenz U; Rininsland F; Ballhausen P; Drews D; Posselt HG
Hum Genet; 1992 Nov; 90(3):303-4. PubMed ID: 1283151
[TBL] [Abstract][Full Text] [Related]
5. 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
Wien Klin Wochenschr; 1995; 107(15):464-9. PubMed ID: 7545856
[TBL] [Abstract][Full Text] [Related]
6. Identification of three novel mutations in the CFTR gene using temperature-optimized non-radioactive conditions for SSCP analysis.
Grade K; Grunewald I; Graupner I; Behrens F; Coutelle C
Hum Genet; 1994 Aug; 94(2):154-8. PubMed ID: 7519167
[TBL] [Abstract][Full Text] [Related]
7. Analysis of the 27 exons and flanking regions of the cystic fibrosis gene: 40 different mutations account for 91.2% of the mutant alleles in southern France.
Claustres M; Laussel M; Desgeorges M; Giansily M; Culard JF; Razakatsara G; Demaille J
Hum Mol Genet; 1993 Aug; 2(8):1209-13. PubMed ID: 7691344
[TBL] [Abstract][Full Text] [Related]
8. A termination mutation (2143delT) in the CFTR gene of German cystic fibrosis patients.
Dörk T; Kälin N; Stuhrmann M; Schmidtke J; Tümmler B
Hum Genet; 1992 Nov; 90(3):279-84. PubMed ID: 1283149
[TBL] [Abstract][Full Text] [Related]
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
Clin Genet; 1993 Jul; 44(1):12-4. PubMed ID: 7691448
[TBL] [Abstract][Full Text] [Related]
10. Identification of the M1101K mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and complete detection of cystic fibrosis mutations in the Hutterite population.
Zielenski J; Fujiwara TM; Markiewicz D; Paradis AJ; Anacleto AI; Richards B; Schwartz RH; Klinger KW; Tsui LC; Morgan K
Am J Hum Genet; 1993 Mar; 52(3):609-15. PubMed ID: 7680525
[TBL] [Abstract][Full Text] [Related]
11. Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutations.
Dörk T; Fislage R; Neumann T; Wulf B; Tümmler B
Hum Genet; 1994 Jan; 93(1):67-73. PubMed ID: 7505767
[TBL] [Abstract][Full Text] [Related]
12. Identification of 12 novel mutations in the CFTR gene.
Audrézet MP; Mercier B; Guillermit H; Quéré I; Verlingue C; Rault G; Férec C
Hum Mol Genet; 1993 Jan; 2(1):51-4. PubMed ID: 7683952
[TBL] [Abstract][Full Text] [Related]
13. Analysis of the CFTR gene in the Spanish population: SSCP-screening for 60 known mutations and identification of four new mutations (Q30X, A120T, 1812-1 G-->A, and 3667del4).
Chillón M; Casals T; Giménez J; Nunes V; Estivill X
Hum Mutat; 1994; 3(3):223-30. PubMed ID: 7517264
[TBL] [Abstract][Full Text] [Related]
14. The occurrence of various non-delta F508 CFTR gene mutations among Hungarian cystic fibrosis patients.
Nemeti M; Johnson JP; Papp Z; Louie E
Hum Genet; 1992 May; 89(2):245-6. PubMed ID: 1375186
[TBL] [Abstract][Full Text] [Related]
15. Screening for cystic fibrosis mutations in southern France: identification of a frameshift mutation and two missense variations.
Claustres M; Gerrard B; Kjellberg P; Desgeorges M; Demaille J; Dean M
Hum Mutat; 1992; 1(4):310-3. PubMed ID: 1284537
[TBL] [Abstract][Full Text] [Related]
16. Two new mutations detected by single-strand conformation polymorphism analysis in cystic fibrosis from Russia.
Ivaschenko TE; Baranov VS; Dean M
Hum Genet; 1993 Mar; 91(1):63-5. PubMed ID: 7681034
[TBL] [Abstract][Full Text] [Related]
17. 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
Hum Genet; 1992 Feb; 88(4):417-25. PubMed ID: 1371263
[TBL] [Abstract][Full Text] [Related]
18. Screening for CF mutations in adult cystic fibrosis patients with a directed and optimized SSCP strategy.
Ravnik-Glavac M; Glavac D; Chernick M; di Sant'Agnese P; Dean M
Hum Mutat; 1994; 3(3):231-8. PubMed ID: 7517265
[TBL] [Abstract][Full Text] [Related]
19. Single-stranded conformation polymorphism analysis of the CFTR gene in Slovenian cystic fibrosis patients: detection of mutations and sequence variations.
Ravnik-Glavac M; Glavac D; Komel R; Dean M
Hum Mutat; 1993; 2(4):286-92. PubMed ID: 7691352
[TBL] [Abstract][Full Text] [Related]
20. A new polymorphism in exon 7 of the cystic fibrosis transmembrane regulator (CFTR) gene.
Petreska L; Koceva S; Gordova-Muratovska A; Efremov GD
Hum Genet; 1995 Apr; 95(4):465-6. PubMed ID: 7535746
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]