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Article

Multiple analysis of three common genetic alterations associated with thrombophilia.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Mar 2000

Pecheniuk N M, Marsh N A, Walsh T P

Abstract excerpt

We have previously reported the use of a novel mini-sequencing protocol for detection of the factor V Leiden variant, the first nucleotide change (FNC) technology. This technology is based on a single nucleotide extension of a primer, which is hybridized immediately adjacent to the site of mutation. The extended nucleotide that carries a reporter molecule (fluorescein) has the power to discriminate the genotype...

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Identifiers

PMID: 10759012

Genes

MTHFR

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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