BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

100 related articles for article (PubMed ID: 9156329)

  • 1. 1283 del A: a novel mutation in exon 8 of the cystic fibrosis gene.
    Bienvenu T; Bousquet S; Lyonnet S; Kaplan JC; Beldjord C
    Hum Hered; 1997; 47(3):173-5. PubMed ID: 9156329
    [No Abstract]   [Full Text] [Related]  

  • 2. A novel frameshift mutation, c.1870delG, in exon 12 of the CFTR gene.
    Seydewitz HH; Gonska T; Mall M; Kueh J
    Hum Mutat; 2000 Sep; 16(3):277. PubMed ID: 10980550
    [No Abstract]   [Full Text] [Related]  

  • 3. Identification of a new frameshift mutation (3724 delG) in exon 19 of the CFTR gene.
    Bienvenu T; Lenoir G; Fonknechten N; Desclaux-Arramond F; Kaplan JC; Beldjord C
    Hum Mutat; 1994; 3(1):69-70. PubMed ID: 7509685
    [No Abstract]   [Full Text] [Related]  

  • 4. A new frameshift mutation 460delG in exon 4 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
    Wagner K; Schneditz P; Rosenkranz W
    Hum Mutat; 1996; 7(2):183. PubMed ID: 8829644
    [No Abstract]   [Full Text] [Related]  

  • 5. Molecular characterization of a frameshift mutation in exon 19 of the CFTR gene.
    Sangiuolo F; Lo Cicero S; Maceratesi P; Quattrucci S; Novelli G; Dallapiccola B
    Hum Mutat; 1993; 2(5):422-4. PubMed ID: 7504970
    [No Abstract]   [Full Text] [Related]  

  • 6. Mutations located in exon 24 of the CFTR gene are associated with a mild cystic fibrosis phenotype.
    Bienvenu T; Viel M; Leroy C; Van Esch H; Fajac I; Dusser D; Hubert D
    Clin Genet; 2003 Sep; 64(3):266-8. PubMed ID: 12919146
    [No Abstract]   [Full Text] [Related]  

  • 7. Cystic fibrosis caused by homozygosity for the CFTR gene mutation 175insT.
    Schaedel C; Schwartz M; Kornfält R; Holmberg L
    Acta Paediatr; 1995 Oct; 84(10):1199-200. PubMed ID: 8563237
    [No Abstract]   [Full Text] [Related]  

  • 8. Cystic fibrosis in a Hispanic adolescent.
    Lin JH; Collaco JM; Paranjape SM
    Pediatr Pulmonol; 2014 Mar; 49(3):E40-1. PubMed ID: 23401342
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel nonsense mutation (Q1291X) in exon 20 of CFTR (ABCC7) gene.
    Feldmann D; Laroze F; Troadec C; Clement A; Tournier G; Couderc R
    Hum Mutat; 2001 Apr; 17(4):356. PubMed ID: 11295849
    [No Abstract]   [Full Text] [Related]  

  • 10. 40 kilobase deletion (CF 40 kb del 4-10) removes exons 4 to 10 of the Cystic Fibrosis Transmembrane Conductance Regulator gene.
    Chevalier-Porst F; Bonardot AM; Chazalette JP; Mathieu M; Bozon D
    Hum Mutat; 1998; Suppl 1():S291-4. PubMed ID: 9452112
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. Two novel frame-shift mutations: 977 insA in exon 6B, and 4016 insT in exon 21, of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
    Cheadle JP; al-Jader LN; Meredith AL
    Hum Mol Genet; 1993 Mar; 2(3):317-9. PubMed ID: 7684644
    [No Abstract]   [Full Text] [Related]  

  • 13. Identification of a novel mutation, 1087delT, in exon 7 of the CFTR gene in a patient with cystic fibrosis.
    Feuillet-Fieux MN; Sermet I; Edelman A; Torossi T; Ferrec M; Guillot M; Lenoir G; Bonnefont JP; Thuillier L
    Hum Mutat; 2000 Jul; 16(1):95. PubMed ID: 10874326
    [No Abstract]   [Full Text] [Related]  

  • 14. Identification of four novel mutations in the cystic fibrosis transmembrane conductance regulator gene: E664X, 2113delA, 306delTAGA, and delta M1140.
    Clavel C; Pennaforte F; Pigeon F; Verlingue C; Birembaut P; Férec C
    Hum Mutat; 1997; 9(4):368-9. PubMed ID: 9101301
    [No Abstract]   [Full Text] [Related]  

  • 15. Severe cystic fibrosis in a Japanese girl caused by two novel CFTR (ABCC7) gene mutations: M152R and 1540del10.
    Morokawa N; Iizuka S; Tanano A; Katsube A; Muraji T; Eto Y; Yoshimura K
    Hum Mutat; 2000 May; 15(5):485. PubMed ID: 10790220
    [No Abstract]   [Full Text] [Related]  

  • 16. Identification of two mutations (S50Y and 4173delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD).
    Zielenski J; Patrizio P; Markiewicz D; Asch RH; Tsui LC
    Hum Mutat; 1997; 9(2):183-4. PubMed ID: 9067761
    [No Abstract]   [Full Text] [Related]  

  • 17. A 2-amino acid insertion mutation (1243insACAAAA) in exon 7 of the CFTR gene.
    Shackleton S; Harris A
    Hum Mutat; 1998; Suppl 1():S156-7. PubMed ID: 9452073
    [No Abstract]   [Full Text] [Related]  

  • 18. A novel frame-shift mutation in exon 4 of the cystic fibrosis gene (435insA) demonstrates the ambiguity of restriction analysis for mutation screening.
    Kälin N; Dörk T; Bozon D; Tümmler B
    Hum Mol Genet; 1992 Oct; 1(7):545-6. PubMed ID: 1284889
    [No Abstract]   [Full Text] [Related]  

  • 19. Novel double mutant CF allele identified in a cystic fibrosis patient with meconium ileus.
    Steffann J; Vidaud D; Bousquet S; Jullien M; Ninot A; Kaplan JC; Beldjord C; Bienvenu T
    Ann Genet; 1998; 41(4):213-5. PubMed ID: 9881185
    [No Abstract]   [Full Text] [Related]  

  • 20. Novel mutation (A141D) in exon 4 of the CFTR gene identified in an Algerian patient.
    Gouya L; Pascaud O; Munck A; Elion J; Denamur E
    Hum Mutat; 1997; 10(1):86-7. PubMed ID: 9222768
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.