Literature DB >> 8838224

Amplification methods in the molecular diagnosis of genetic diseases.

J M Ben-Ezra1.   

Abstract

The ability to amplify DNA by the polymerase chain reaction (PCR) technique has revolutionized our ability to test for genetic mutations. Many different assay systems are available for analyzing the amplified DNA and RNA. These techniques can be performed easily on material from adults, children, fetuses, and even single cells from blastomeres and polar bodies. The detection rate of the screening test, as well as the frequency of the mutation in the study population and the technical limitations of the procedure, will determine the usefulness of a positive or negative result. Preimplantation testing provides a paradigm for the ease of use of PCR-based testing, yet also underscores the problems encountered with genetic screening because of the multitude of possible mutations and the possible misinterpretation of results.

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Year:  1995        PMID: 8838224

Source DB:  PubMed          Journal:  Clin Lab Med        ISSN: 0272-2712            Impact factor:   1.935


  2 in total

1.  Goals and objectives for molecular pathology education in residency programs. The Association for Molecular Pathology Training and Education Committee.

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Journal:  J Mol Diagn       Date:  1999-11       Impact factor: 5.568

2.  Investigate the correlation between clinical sign and symptoms and the presence of P. gingivalis, T. denticola, and T. forsythia individually or as a "Red complex" by a multiplex PCR method.

Authors:  Tulsi Hasmukhrai Sanghavi; Nimisha Shah; Ruchi Rani Shah; Akta Sanghavi
Journal:  J Conserv Dent       Date:  2014-11
  2 in total

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