271 related articles for article (PubMed ID: 7691353)
1. Simultaneous detection of the two prevalent mutations in the cystic fibrosis gene in Reunion Island.
Bienvenu T; Bousquet S; Herbulot C; Cartault F; Kaplan JC; Beldjord C
Hum Mutat; 1993; 2(4):306-8. PubMed ID: 7691353
[TBL] [Abstract][Full Text] [Related]
2. Fluorescence-based oligonucleotide ligation assay for analysis of cystic fibrosis transmembrane conductance regulator gene mutations.
Eggerding FA; Iovannisci DM; Brinson E; Grossman P; Winn-Deen ES
Hum Mutat; 1995; 5(2):153-65. PubMed ID: 7538376
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. [A molecular study of the delta-F508 mutation and genetic analysis of a sample of cystic fibrosis patients].
Orozco L; Lezana JL; Chávez M; Valdez H; Moreno M; Carnevale A
Bol Med Hosp Infant Mex; 1993 Jul; 50(7):457-62. PubMed ID: 7689846
[TBL] [Abstract][Full Text] [Related]
6. A frame-shift mutation in the cystic fibrosis gene.
White MB; Amos J; Hsu JM; Gerrard B; Finn P; Dean M
Nature; 1990 Apr; 344(6267):665-7. PubMed ID: 1691449
[TBL] [Abstract][Full Text] [Related]
7. A rapid, efficient, and sensitive assay for simultaneous detection of multiple cystic fibrosis mutations.
Costes B; Fanen P; Goossens M; Ghanem N
Hum Mutat; 1993; 2(3):185-91. PubMed ID: 7689902
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [Molecular-genetic analysis of certain mutations of the "cystic fibrosis gene" in Moldavia. Characteristics of molecular markers and their linkage with various mutations].
Gimbovskaia SD; Kalinin VN; Ivashchenko TE; Baranov VS
Genetika; 1994 Dec; 30(12):1616-20. PubMed ID: 7534245
[TBL] [Abstract][Full Text] [Related]
10. Identification of rare and novel mutations in the CFTR genes of CF patients in southern England.
Shackleton S; Hull J; Dear S; Seller A; Thomson A; Harris A
Hum Mutat; 1994; 3(2):141-51. PubMed ID: 7515303
[TBL] [Abstract][Full Text] [Related]
11. Identification of four new mutations in the cystic fibrosis transmembrane conductance regulator gene: I148T, L1077P, Y1092X, 2183AA-->G.
Bozon D; Zielenski J; Rininsland F; Tsui LC
Hum Mutat; 1994; 3(3):330-2. PubMed ID: 7517268
[No Abstract] [Full Text] [Related]
12. DNA analysis of cystic fibrosis in Brazil by direct PCR amplification from Guthrie cards.
Raskin S; Phillips JA; Krishnamani MR; Vnencak-Jones C; Parker RA; Rozov T; Cardieri JM; Marostica P; Abreu F; Giugliani R
Am J Med Genet; 1993 Jul; 46(6):665-9. PubMed ID: 8362909
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Cystic fibrosis at the Reunion Island (France): spectrum of mutations and genotype-phenotype for the Y122X mutation.
Duguépéroux I; Bellis G; Lesure JF; Renouil M; Flodrops H; De Braekeleer M
J Cyst Fibros; 2004 Aug; 3(3):185-8. PubMed ID: 15463906
[TBL] [Abstract][Full Text] [Related]
15. Detection of over 98% cystic fibrosis mutations in a Celtic population.
Férec C; Audrezet MP; Mercier B; Guillermit H; Moullier P; Quere I; Verlingue C
Nat Genet; 1992 Jun; 1(3):188-91. PubMed ID: 1284639
[TBL] [Abstract][Full Text] [Related]
16. A cystic fibrosis patient with delta F508, G542X and a deletion at the D7S8 locus.
Wagner K; Greil I; Schneditz P; Pommer M; Rosenkranz W
Hum Mutat; 1994; 3(3):327-9. PubMed ID: 7517267
[No Abstract] [Full Text] [Related]
17. Prevalence of cystic fibrosis mutations in the East German population.
Coutelle C; Brückner R; Grade K; Behrens F; Gedschold J; Hein J; Szibor R; Bauer I; Brock J; Graupner I
Hum Mutat; 1992; 1(2):109-12. PubMed ID: 1301197
[TBL] [Abstract][Full Text] [Related]
18. Population screening of F508del (DeltaF508), the most frequent mutation in the CFTR gene associated with cystic fibrosis in Argentina.
Roqué M; Godoy CP; Castellanos M; Pusiol E; Mayorga LS
Hum Mutat; 2001 Aug; 18(2):167. PubMed ID: 11462248
[TBL] [Abstract][Full Text] [Related]
19. [Cystic fibrosis in Asturias: an elevated frequency of the delta F508 mutation].
Coto E; Bousoño C; Menéndez MJ; Cue R; Toral JF; Benavides A; Hernando I; Plasencia A; López-Larrea C
Med Clin (Barc); 1994 Nov; 103(18):681-3. PubMed ID: 7808073
[TBL] [Abstract][Full Text] [Related]
20. Molecular diagnosis of cystic fibrosis.
Kant JA; Mifflin TE; McGlennen R; Rice E; Naylor E; Cooper DL
Clin Lab Med; 1995 Dec; 15(4):877-98. PubMed ID: 8838228
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
