413 related articles for article (PubMed ID: 9829908)
1. Use of denaturing gradient gel blots to screen for point mutations in the factor VIII gene.
Laprise SL; Mak EK; Killoran KA; Layman LC; Gray MR
Hum Mutat; 1998; 12(6):393-402. PubMed ID: 9829908
[TBL] [Abstract][Full Text] [Related]
2. The use of denaturing gradient gel electrophoresis to screen for DNA sequence polymorphisms in the human factor VIII gene.
Collins M; Wolf SF; Haines LL; Mitsock L
Electrophoresis; 1989; 10(5-6):390-6. PubMed ID: 2569966
[TBL] [Abstract][Full Text] [Related]
3. A directed search for mutations in hemophilia A using restriction enzyme analysis and denaturing gradient gel electrophoresis. A study of seven exons in the factor VIII gene of 170 cases.
Lavergne JM; Bahnak BR; Vidaud M; Laurian Y; Meyer D
Nouv Rev Fr Hematol (1978); 1992; 34(1):85-91. PubMed ID: 1523102
[TBL] [Abstract][Full Text] [Related]
4. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
5. Precise carrier diagnosis in families with haemophilia A: use of conformation sensitive gel electrophoresis for mutation screening and polymorphism analysis.
Williams IJ; Abuzenadah A; Winship PR; Preston FE; Dolan G; Wright J; Peake IR; Goodeve AC
Thromb Haemost; 1998 Apr; 79(4):723-6. PubMed ID: 9569180
[TBL] [Abstract][Full Text] [Related]
6. Detection by denaturing gradient gel electrophoresis of an Arg1689Cys mutation in a Chinese patient with mild hemophilia A.
Ruan C; Gu J; Lavergne JM; Meyer D
Chin Med J (Engl); 1997 Feb; 110(2):96-9. PubMed ID: 9594277
[TBL] [Abstract][Full Text] [Related]
7. Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions.
Jayandharan G; Shaji RV; Baidya S; Nair SC; Chandy M; Srivastava A
Haemophilia; 2005 Sep; 11(5):481-91. PubMed ID: 16128892
[TBL] [Abstract][Full Text] [Related]
8. [Application studies on the gene diagnosis and carrier detection of hemophilia A by using polymerase chain reaction-conformation sensitive gel electrophoresis].
Lillicrap D; He GP; Leggo J; Liu YS; Tong XH; Zhou GX; Luo LH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):393-9. PubMed ID: 20017302
[TBL] [Abstract][Full Text] [Related]
9. [A novel missense mutation in the B domain of factor VIII causes severe hemophilia A].
Liu J; Zhang Y; Wang H
Zhonghua Xue Ye Xue Za Zhi; 1998 Sep; 19(9):458-60. PubMed ID: 11189482
[TBL] [Abstract][Full Text] [Related]
10. Long distance PCR in detection of inversion mutations of F8C gene in hemophilia A patients.
Poláková H; Zmetáková I; Kádasi L
Gen Physiol Biophys; 2003 Jun; 22(2):243-53. PubMed ID: 14699993
[TBL] [Abstract][Full Text] [Related]
11. Hemophilia B carrier determination based on family-specific mutation detection by DNA single-strand conformation analysis.
Poon MC; Anand S; Fraser BM; Hoar DI; Sinclair GD
J Lab Clin Med; 1993 Jul; 122(1):55-63. PubMed ID: 8320491
[TBL] [Abstract][Full Text] [Related]
12. Double strand conformation polymorphism (DSCP) detects two point mutations at codon 280 (AAC-->ATC) and at codon 431 (TAC-->AAC) of the blood coagulation factor VIII gene.
Pieneman WC; Reitsma PH; Briët E
Thromb Haemost; 1993 May; 69(5):473-5. PubMed ID: 8322269
[TBL] [Abstract][Full Text] [Related]
13. Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A.
Bogdanova N; Markoff A; Pollmann H; Nowak-Göttl U; Eisert R; Dworniczak B; Eigel A; Horst J
Hum Mutat; 2002 Sep; 20(3):236-7. PubMed ID: 12204009
[TBL] [Abstract][Full Text] [Related]
14. Characterization of genetic defects of hemophilia A in patients of Chinese origin.
Lin SW; Lin SR; Shen MC
Genomics; 1993 Dec; 18(3):496-504. PubMed ID: 8307558
[TBL] [Abstract][Full Text] [Related]
15. High throughput mutation screening of the factor VIII gene (F8C) in hemophilia A: 37 novel mutations and genotype-phenotype correlation.
Citron M; Godmilow L; Ganguly T; Ganguly A
Hum Mutat; 2002 Oct; 20(4):267-74. PubMed ID: 12325022
[TBL] [Abstract][Full Text] [Related]
16. Mutation detection by denaturing gradient gel electrophoresis (DGGE).
Fodde R; Losekoot M
Hum Mutat; 1994; 3(2):83-94. PubMed ID: 8199599
[TBL] [Abstract][Full Text] [Related]
17. Single-step DGGE-based mutation scanning of the p53 gene: application to genetic diagnosis of colorectal cancer.
Guldberg P; Nedergaard T; Nielsen HJ; Olsen AC; Ahrenkiel V; Zeuthen J
Hum Mutat; 1997; 9(4):348-55. PubMed ID: 9101296
[TBL] [Abstract][Full Text] [Related]
18. Denaturing gradient gel electrophoresis (DGGE) increases resolution and informativity of Alu-directed inter-repeat PCR.
van Orsouw NJ; Li D; Vijg J
Mol Cell Probes; 1997 Apr; 11(2):95-101. PubMed ID: 9160323
[TBL] [Abstract][Full Text] [Related]
19. Implications of gene sequencing in the direct diagnosis of hemophilia by PCR-RFLP.
Vidal F; Farssac E; Altisent C; Puig L; Gallardo D
Haematologica; 2002 Jan; 87(1):109-10. PubMed ID: 11801473
[No Abstract] [Full Text] [Related]
20. Rapid hemophilia A molecular diagnosis by a simple DNA sequencing procedure: identification of 14 novel mutations.
Vidal F; Farssac E; Altisent C; Puig L; Gallardo D
Thromb Haemost; 2001 Apr; 85(4):580-3. PubMed ID: 11341489
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
