Single-well genotyping of diallelic sequence variations by a two-color ELISA-based oligonucleotide ligation assay.

Single nucleotide substitutions and unique insertions/deletions are the most common form of DNA sequence variation and disease-causing mutation in the human genome. Because of the biological and medical importance of these variations, a wide array of methods have been developed for their typing. We...

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Detalhes bibliográficos

Publicado no:	Nucleic Acids Res
Principais autores:	Tobe, V O, Taylor, S L, Nickerson, D A
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Oxford University Press 1996
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC146169/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8871551/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/24.19.3728
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