| 1 |
A simple, high sensitivity mutation screening using Ampligase mediated T7 endonuclease I and Surveyor nuclease with microfluidic capillary electrophoresis
Huang MC, Cheong WC, Lim LS, Li MH
Electrophoresis, 33(5), 788, 2012 |
| 2 |
A novel mutation screening system for Ehlers-Danlos Syndrome, vascular type by high-resolution melting curve analysis in combination with small amplicon genotyping using genomic DNA
Naing BT, Watanabe A, Shimada T
Biochemical and Biophysical Research Communications, 405(3), 368, 2011 |
| 3 |
Development of a simple and highly sensitive mutation screening system by enzyme mismatch cleavage with optimized conditions for standard laboratories
Tsuji T, Niida Y
Electrophoresis, 29(7), 1473, 2008 |
| 4 |
Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations
Fauser S, Luberichs J, Besch D, Leo-Kottler B
Biochemical and Biophysical Research Communications, 295(2), 342, 2002 |
| 5 |
Fluorescence-based single-strand conformation polymorphism analysis of mutations by capillary electrophoresis
Walz T, Geisel J, Bodis M, Knapp JP, Herrmann W
Electrophoresis, 21(2), 375, 2000 |
