Minisequencing: a specific tool for DNA analysis and diagnostics on oligonucleotide arrays. (Q40893213)

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4 November 2019

title

Minisequencing: a specific tool for DNA analysis and diagnostics on oligonucleotide arrays (English)

1 reference

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nucleic acid sequence analysis

4 November 2019

main subject

1 reference

2

1 reference

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3

A Metspalu

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4 November 2019

Ann-Christine Syvänen

series ordinal

5

object named as

A C Syvänen

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4 November 2019

author name string

T Pastinen

series ordinal

1

1 reference

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4 November 2019

L Peltonen

series ordinal

4

1 reference

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publication date

1 June 1997

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4 November 2019

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volume

7

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issue

6

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page(s)

606-614

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Finnish type of low density lipoprotein receptor gene mutation (FH-Helsinki) deletes exons encoding the carboxy-terminal part of the receptor and creates an internalization-defective phenotype

4 November 2019

cites work

1 reference

Mutation in blood coagulation factor V associated with resistance to activated protein C.

21 January 2018

1 reference

Accessing genetic information with high-density DNA arrays.

21 January 2018

1 reference

Detection of sickle cell beta S-globin allele by hybridization with synthetic oligonucleotides

21 January 2018

1 reference

Light-directed, spatially addressable parallel chemical synthesis

21 January 2018

1 reference

Direct fluorescence analysis of genetic polymorphisms by hybridization with oligonucleotide arrays on glass supports

21 January 2018

1 reference

Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis

21 January 2018

1 reference

The familial hypercholesterolemia (FH)-North Karelia mutation of the low density lipoprotein receptor gene deletes seven nucleotides of exon 6 and is a common cause of FH in Finland

21 January 2018

1 reference

Extensive polymorphisms observed in HIV-1 clade B protease gene using high-density oligonucleotide arrays.

21 January 2018

1 reference

Identification of a common mutation in Finnish patients with nonketotic hyperglycinemia

21 January 2018

1 reference

Direct detection of nucleic acid hybridization on the surface of a charge coupled device

21 January 2018

1 reference

Light-directed synthesis of high-density oligonucleotide arrays using semiconductor photoresists

21 January 2018

1 reference

At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.

21 January 2018

1 reference

Light-generated oligonucleotide arrays for rapid DNA sequence analysis

21 January 2018

1 reference

Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes

21 January 2018

1 reference

Quantitative monitoring of gene expression patterns with a complementary DNA microarray

21 January 2018

1 reference

Parallel human genome analysis: microarray-based expression monitoring of 1000 genes

21 January 2018

1 reference

Karyotyping human chromosomes by combinatorial multi-fluor FISH.

21 January 2018

1 reference

A single residue in DNA polymerases of the Escherichia coli DNA polymerase I family is critical for distinguishing between deoxy- and dideoxyribonucleotides

21 January 2018

1 reference

Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1101/GR.7.6.606

1 reference

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4 November 2019

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