(Q40871599)

24 September 2017

1 reference

title

DNA variation and the future of human genetics (English)

1 reference

24 September 2017

1 reference

Schafer AJ

1

1 reference

PubMed ID

9447590

24 September 2017

Hawkins JR

series ordinal

2

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24 September 2017

1 January 1998

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24 September 2017

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24 September 2017

16

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24 September 2017

33-39

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24 September 2017

1

1 reference

https://scigraph.springernature.com/pub.10.1038/nbt0198-33

24 September 2017

0 references

cites work

Molecular genetic basis of the histo-blood group ABO system.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

The Bloom's syndrome gene product is homologous to RecQ helicases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

A genome-wide search for human type 1 diabetes susceptibility genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

Multifactorial inheritance in type 1 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

Polygenic disease: methods for mapping complex disease traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

Positional cloning reaches maturity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

High Association of an HL-A Antigen, W27, with Ankylosing Spondylitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

Use of siblings as controls in case-control association studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

Practical methods of mutation detection

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

Viable offspring derived from fetal and adult mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

Ultrarapid mutation detection by multiplex, solid-phase chemical cleavage

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

Potassium permanganate and tetraethylammonium chloride are a safe and effective substitute for osmium tetroxide in solid-phase fluorescent chemical cleavage of mismatch

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

Mutation detection with MutH, MutL, and MutS mismatch repair proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

A pre-Columbian Y chromosome-specific transition and its implications for human evolutionary history

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

DNA sequencing by delayed extraction-matrix-assisted laser desorption/ionization time of flight mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

Variations in Human Serum β-Globulins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

An estimate of unique DNA sequence heterozygosity in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Hypervariable 'minisatellite' regions in human DNA.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Variable number of tandem repeat (VNTR) markers for human gene mapping

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Genetic dissection of complex traits

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

The generalized sib pair IBD distribution: its use in the detection of linkage

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Fragile X genotype characterized by an unstable region of DNA.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

The maddening hunt for madness genes

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Positional cloning moves from perditional to traditional

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Association and linkage: complementary strategies for complex disorders

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Ankylosing spondylitis and HL-A 27.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

The use of a genetic map of biallelic markers in linkage studies

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

The rapid detection of unknown mutations in nucleic acids.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

How sensitive is PCR-SSCP?

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Analysis of factor VIII mRNA reveals defects in everyone of 28 haemophilia A patients

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Point mutations in the dystrophin gene

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Error analysis in manual and automated DNA sequencing

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Mutation detection by solid phase primer extension

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

To affinity ... and beyond!

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Specific-locus test shows ethylnitrosourea to be the most potent mutagen in the mouse

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Detecting single base substitutions as heteroduplex polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: correspondence with melting theory

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Temperature-gradient gel electrophoresis of nucleic acids: analysis of conformational transitions, sequence variations, and protein-nucleic acid interactions.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Detection of single base substitutions by ribonuclease cleavage at mismatches in RNA:DNA duplexes.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Detection of 81 of 81 known mouse beta-globin promoter mutations with T4 endonuclease VII--the EMC method

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Towards fully automated genome-wide polymorphism screening

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Light-generated oligonucleotide arrays for rapid DNA sequence analysis

1 reference

https://api.crossref.org/works/10.1038%2FNBT0198-33

7 January 2021

Identifiers

DOI

10.1038/NBT0198-33

1 reference

PubMed ID

9447590

Dimensions Publication ID

24 September 2017

0 references

1 reference

PubMed ID

9447590