118 related articles for article (PubMed ID: 8510541)
1. Polymerase chain reaction amplification of specific alleles: a general method of detection of mutations, polymorphisms, and haplotypes.
Bottema CD; Sarkar G; Cassady JD; Ii S; Dutton CM; Sommer SS
Methods Enzymol; 1993; 218():388-402. PubMed ID: 8510541
[No Abstract] [Full Text] [Related]
2. Simultaneous detection of multiple single-base alleles at a polymorphic site.
Dutton C; Sommer SS
Biotechniques; 1991 Dec; 11(6):700-2. PubMed ID: 1809318
[TBL] [Abstract][Full Text] [Related]
3. Removal of DNA contamination in polymerase chain reaction reagents by ultraviolet irradiation.
Sarkar G; Sommer SS
Methods Enzymol; 1993; 218():381-8. PubMed ID: 8318118
[No Abstract] [Full Text] [Related]
4. Identification of factor IX mutations in haemophilia B: application of polymerase chain reaction and single strand conformation analysis.
Fraser BM; Poon MC; Hoar DI
Hum Genet; 1992 Feb; 88(4):426-30. PubMed ID: 1740319
[TBL] [Abstract][Full Text] [Related]
5. PCR amplification of specific alleles: rapid detection of known mutations and polymorphisms.
Bottema CD; Sommer SS
Mutat Res; 1993 Jul; 288(1):93-102. PubMed ID: 7686270
[TBL] [Abstract][Full Text] [Related]
6. Polymerase chain reaction detection of the Dde I polymorphism in the factor 9 gene for fragile X linkage analysis.
Dobkin CS; Driscoll MC; Ferrando C
Am J Med Genet; 1991; 38(2-3):378-9. PubMed ID: 2018077
[TBL] [Abstract][Full Text] [Related]
7. Haplotyping by double PCR amplification of specific alleles.
Sarkar G; Sommer SS
Biotechniques; 1991 Apr; 10(4):436, 438, 440. PubMed ID: 1831030
[TBL] [Abstract][Full Text] [Related]
8. PCR amplification of specific alleles (PASA) is a general method for rapidly detecting known single-base changes.
Sommer SS; Groszbach AR; Bottema CD
Biotechniques; 1992 Jan; 12(1):82-7. PubMed ID: 1734929
[TBL] [Abstract][Full Text] [Related]
9. New strategy for detection of ALDH2 mutant.
Harada S; Zhang S
Alcohol Alcohol Suppl; 1993; 1A():11-3. PubMed ID: 8141918
[TBL] [Abstract][Full Text] [Related]
10. Characterization of factor IX defects in hemophilia B patients.
Thompson AR; Chen SH
Methods Enzymol; 1993; 222():143-69. PubMed ID: 8412791
[No Abstract] [Full Text] [Related]
11. Haplotype analysis of identical factor IX mutants using PCR.
Green PM; Montandon AJ; Ljung R; Nilsson IM; Giannelli F
Thromb Haemost; 1992 Jan; 67(1):66-9. PubMed ID: 1615486
[TBL] [Abstract][Full Text] [Related]
12. A mutation in the 3' untranslated region of the factor IX gene in four families with hemophilia B.
Vielhaber E; Jacobson DP; Ketterling RP; Liu JZ; Sommer SS
Hum Mol Genet; 1993 Aug; 2(8):1309-10. PubMed ID: 8401514
[No Abstract] [Full Text] [Related]
13. A novel blocker-PCR method for detection of rare mutant alleles in the presence of an excess amount of normal DNA.
Seyama T; Ito T; Hayashi T; Mizuno T; Nakamura N; Akiyama M
Nucleic Acids Res; 1992 May; 20(10):2493-6. PubMed ID: 1598207
[TBL] [Abstract][Full Text] [Related]
14. Detection of polymorphisms at cytosine phosphoguanadine dinucleotides and diagnosis of haemophilia B carriers.
Winship PR; Rees DJ; Alkan M
Lancet; 1989 Mar; 1(8639):631-4. PubMed ID: 2564457
[TBL] [Abstract][Full Text] [Related]
15. Genetic polymorphism of debrisoquine oxidation: restriction fragment analysis and allele-specific amplification of mutant alleles of CYP2D6.
Heim MH; Meyer UA
Methods Enzymol; 1991; 206():173-83. PubMed ID: 1686063
[No Abstract] [Full Text] [Related]
16. Double-stranded DNA segments can efficiently prime the amplification of human genomic DNA.
Sarkar G; Sommer SS
Nucleic Acids Res; 1992 Sep; 20(18):4937-8. PubMed ID: 1408814
[No Abstract] [Full Text] [Related]
17. Twenty-four novel hemophilia B mutations revealed by rapid scanning of the whole factor IX gene in a French population sample.
Ghanem N; Costes B; Martin J; Vidaud M; Rothschild C; Foyer-Gazengel C; Goossens M
Eur J Hum Genet; 1993; 1(2):144-55. PubMed ID: 8055323
[TBL] [Abstract][Full Text] [Related]
18. Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations.
Wedell A; Ritzén EM; Haglund-Stengler B; Luthman H
Proc Natl Acad Sci U S A; 1992 Aug; 89(15):7232-6. PubMed ID: 1496017
[TBL] [Abstract][Full Text] [Related]
19. Improved method for direct PCR amplification from whole blood.
McCusker J; Dawson MT; Noone D; Gannon F; Smith T
Nucleic Acids Res; 1992 Dec; 20(24):6747. PubMed ID: 1480499
[No Abstract] [Full Text] [Related]
20. The ornithine transcarbamylase gene: new "private" mutations in four patients and study of a polymorphism.
Tuchman M; Plante RJ; Giguère Y; Lemieux B
Hum Mutat; 1994; 3(3):318-20. PubMed ID: 8019569
[No Abstract] [Full Text] [Related]
[Next] [New Search]
