92 related articles for article (PubMed ID: 9094125)
1. Making the perfect mismatch.
Baumbach L
Nat Biotechnol; 1997 Apr; 15(4):318. PubMed ID: 9094125
[No Abstract] [Full Text] [Related]
2. Multi-mutation screening using PCR and ligation--principles and applications.
Winn-Deen ES
Trends Biotechnol; 1996 Apr; 14(4):112-4. PubMed ID: 8936430
[No Abstract] [Full Text] [Related]
3. Chemical cleavage of mismatch: a new look at an established method.
Ellis TP; Humphrey KE; Smith MJ; Cotton RG
Hum Mutat; 1998; 11(5):345-53. PubMed ID: 9600452
[TBL] [Abstract][Full Text] [Related]
4. Identification of coding single nucleotide polymorphisms and mutations by combination of genome tiling arrays and enrichment/depletion of mismatch cDNAs.
Liu MM; Weissman SM; Tang L
Anal Biochem; 2006 Sep; 356(1):117-24. PubMed ID: 16777053
[TBL] [Abstract][Full Text] [Related]
5. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
El-Gawhary S; El-Shafie S; Niazi M; Aziz M; El-Beshlawy A
Hemoglobin; 2007; 31(1):63-9. PubMed ID: 17365006
[TBL] [Abstract][Full Text] [Related]
6. Allele-specific oligonucleotide PCR.
Green EK
Methods Mol Biol; 2002; 187():47-50. PubMed ID: 12013750
[No Abstract] [Full Text] [Related]
7. Approaches to identify genes for complex human diseases: lessons from Mendelian disorders.
Dean M
Hum Mutat; 2003 Oct; 22(4):261-74. PubMed ID: 12955713
[TBL] [Abstract][Full Text] [Related]
8. COLD-PCR: a new platform for highly improved mutation detection in cancer and genetic testing.
Li J; Makrigiorgos GM
Biochem Soc Trans; 2009 Apr; 37(Pt 2):427-32. PubMed ID: 19290875
[TBL] [Abstract][Full Text] [Related]
9. ["Heredity:0?" Human genes on the examination table].
Landegren U
Lakartidningen; 1996 Jun; 93(26-27):2495-8. PubMed ID: 8684079
[No Abstract] [Full Text] [Related]
10. MLPA and MAPH: new techniques for detection of gene deletions.
Sellner LN; Taylor GR
Hum Mutat; 2004 May; 23(5):413-9. PubMed ID: 15108271
[TBL] [Abstract][Full Text] [Related]
11. [Exome sequencing applied to monogenic disorders].
Criqui A; Baulande S
Med Sci (Paris); 2010 May; 26(5):452-4. PubMed ID: 20510136
[No Abstract] [Full Text] [Related]
12. Application of the TaqMan-PCR for genotyping of the prothrombin G20210A mutation and of the thermolabile methylenetetrahydrofolate reductase mutation.
Happich D; Madlener K; Schwaab R; Hanfland P; Pötzsch B
Thromb Haemost; 2000 Jul; 84(1):144-5. PubMed ID: 10928490
[No Abstract] [Full Text] [Related]
13. Biotechnology and molecular diagnostics.
Gulino A
Forum (Genova); 1999; 9(3 Suppl 3):37-46. PubMed ID: 10607845
[TBL] [Abstract][Full Text] [Related]
14. MutS as a tool for mutation detection.
Stanisławska-Sachadyn A; Sachadyn P
Acta Biochim Pol; 2005; 52(3):575-83. PubMed ID: 16082411
[TBL] [Abstract][Full Text] [Related]
15. [Molecular biology in medicine. X. DNA chips].
Gamba G
Rev Invest Clin; 1997; 49(4):339-42. PubMed ID: 9708001
[No Abstract] [Full Text] [Related]
16. Highly selective isolation of unknown mutations in diverse DNA fragments: toward new multiplex screening in cancer.
Chakrabarti S; Price BD; Tetradis S; Fox EA; Zhang Y; Maulik G; Makrigiorgos GM
Cancer Res; 2000 Jul; 60(14):3732-7. PubMed ID: 10919642
[TBL] [Abstract][Full Text] [Related]
17. Universal DNA microarray method for multiplex detection of low abundance point mutations.
Gerry NP; Witowski NE; Day J; Hammer RP; Barany G; Barany F
J Mol Biol; 1999 Sep; 292(2):251-62. PubMed ID: 10493873
[TBL] [Abstract][Full Text] [Related]
18. Patenting DNA: just when you thought it was safe.
Chahine KG
Nat Biotechnol; 1997 Jun; 15(6):586-8. PubMed ID: 9181584
[No Abstract] [Full Text] [Related]
19. Real-time quantitative allele discrimination assay using 3' locked nucleic acid primers for detection of low-percentage mosaic mutations.
Maertens O; Legius E; Speleman F; Messiaen L; Vandesompele J
Anal Biochem; 2006 Dec; 359(1):144-6. PubMed ID: 16962063
[No Abstract] [Full Text] [Related]
20. Two-round allele specific-polymerase chain reaction: a simple and highly sensitive method for JAK2V617F mutation detection.
Kannim S; Thongnoppakhun W; Auewarakul CU
Clin Chim Acta; 2009 Mar; 401(1-2):148-51. PubMed ID: 19135044
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
