(Q38289955)

1 September 2017

title

Rapid genotyping of single nucleotide polymorphisms using novel minor groove binding DNA oligonucleotides (MGB probes). (English)

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single-nucleotide polymorphism

1 September 2017

main subject

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Jacques B de Kok

1

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1 September 2017

Erwin T G Wiegerinck

series ordinal

2

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1 September 2017

Belinda A J Giesendorf

series ordinal

3

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1 September 2017

Dorine W Swinkels

series ordinal

4

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1 September 2017

publication date

1 May 2002

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1 September 2017

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1 September 2017

volume

19

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1 September 2017

issue

5

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1 September 2017

page(s)

554-559

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Efficient priming of PCR with short oligonucleotides conjugated to a minor groove binder

1 September 2017

cites work

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https://api.crossref.org/works/10.1002%2FHUMU.10076

Screening for hemochromatosis. A public health perspective

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10076

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10076

Dissociation kinetics of 19 base paired oligonucleotide-DNA duplexes containing different single mismatched base pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10076

3'-minor groove binder-DNA probes increase sequence specificity at PCR extension temperatures

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10076

Mode of action and application of Scorpion primers to mutation detection

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10076

A Pilot C282Y Hemochromatosis Screening in Italian Newborns by TaqMan™ Technology

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10076

Integrated amplification and detection of the C677T point mutation in the methylenetetrahydrofolate reductase gene by fluorescence resonance energy transfer and probe melting curves

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10076

Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10076

Allelic discrimination using fluorogenic probes and the 5' nuclease assay

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10076

Multicolor molecular beacons for allele discrimination

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10076

21 January 2018

Identifiers

DOI

10.1002/HUMU.10076

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1 September 2017

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