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4. Systematic use of automated fluorescence-based sequence analysis of amplified genomic DNA for rapid detection of point mutations. Tamary H; Surrey S; Kirschmann H; Shalmon L; Zaizov R; Schwartz E; Rappaport EF Am J Hematol; 1994 Jun; 46(2):127-33. PubMed ID: 8172179 [TBL] [Abstract][Full Text] [Related]
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7. Orphan peak analysis: a novel method for detection of point mutations using an automated fluorescence DNA sequencer. Hattori M; Shibata A; Yoshioka K; Sakaki Y Genomics; 1993 Feb; 15(2):415-7. PubMed ID: 8449509 [TBL] [Abstract][Full Text] [Related]
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11. Semiautomated assessment of loss of heterozygosity and replication error in tumors. Canzian F; Salovaara R; Hemminki A; Kristo P; Chadwick RB; Aaltonen LA; de la Chapelle A Cancer Res; 1996 Jul; 56(14):3331-7. PubMed ID: 8764130 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Efficient detection of point mutations on color-coded strands of target DNA. Verpy E; Biasotto M; Meo T; Tosi M Proc Natl Acad Sci U S A; 1994 Mar; 91(5):1873-7. PubMed ID: 8127898 [TBL] [Abstract][Full Text] [Related]
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