Literature DB >> 8019553

Detection of point mutations by solid-phase methods.

A C Syvänen1, U Landegren.   

Abstract

Several techniques exist that permit the efficient distinction among characterized DNA sequence variants. In this review we discuss a number of such analytic procedures. These techniques all take advantage of a variety solid supports to prepare and analyze reaction products. The described diagnostic principles are now being applied for the development of miniaturized assay formats, suitable for automated detection of large sets of sequences in clinical samples.

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Year:  1994        PMID: 8019553     DOI: 10.1002/humu.1380030303

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  4 in total

1.  Real-time closed tube single nucleotide polymorphism (SNP) quantification in pooled samples by quencher extension (QEXT).

Authors:  Knut Rudi; Askild L Holck
Journal:  Nucleic Acids Res       Date:  2003-10-01       Impact factor: 16.971

2.  Testing the feasibility of DNA typing for human identification by PCR and an oligonucleotide ligation assay.

Authors:  C Delahunty; W Ankener; Q Deng; J Eng; D A Nickerson
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

3.  Molecularly defined adult-type hypolactasia in school-aged children with a previous history of cow's milk allergy.

Authors:  Heli Rasinpera; Kristiina Saarinen; Anna Pelkonen; Irma Jarvela; Erkki Savilahti; Kaija-Leena Kolho
Journal:  World J Gastroenterol       Date:  2006-04-14       Impact factor: 5.742

4.  A genetic test which can be used to diagnose adult-type hypolactasia in children.

Authors:  H Rasinperä; E Savilahti; N S Enattah; M Kuokkanen; N Tötterman; H Lindahl; I Järvelä; K-L Kolho
Journal:  Gut       Date:  2004-11       Impact factor: 23.059

  4 in total

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