(Q34869723)

5 August 2017

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse (English)

1 reference

single-nucleotide polymorphism

5 August 2017

1 reference

10

Neal G Copeland

1 reference

5 August 2017

11

Nancy A Jenkins

1 reference

5 August 2017

Tim Wiltshire

1

1 reference

5 August 2017

Mathew T Pletcher

2

1 reference

5 August 2017

Serge Batalov

3

1 reference

5 August 2017

S Whitney Barnes

4

1 reference

5 August 2017

Lisa M Tarantino

5

1 reference

5 August 2017

Michael P Cooke

6

1 reference

5 August 2017

Hua Wu

7

1 reference

5 August 2017

Kevin Smylie

8

1 reference

5 August 2017

Andrey Santrosyan

9

1 reference

5 August 2017

Francis Kalush

12

1 reference

5 August 2017

Richard J Mural

13

1 reference

5 August 2017

Richard J Glynne

14

1 reference

5 August 2017

Steve A Kay

15

1 reference

5 August 2017

Mark D Adams

16

1 reference

5 August 2017

Colin F Fletcher

17

1 reference

5 August 2017

language of work or name

English

0 references

publication date

28 February 2003

1 reference

Proceedings of the National Academy of Sciences of the United States of America

5 August 2017

1 reference

5 August 2017

100

1 reference

5 August 2017

3380-3385

1 reference

5 August 2017

6

1 reference

The structure of haplotype blocks in the human genome

5 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152301

BLAT—The BLAST-Like Alignment Tool

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152301

The Celera Discovery System.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152301

Map Manager QTX, cross-platform software for genetic mapping

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152301

Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152301

Linkage disequilibrium in the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152301

Genealogies of mouse inbred strains

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152301

A YAC-based physical map of the mouse genome.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152301

Targeted disruption of the mouse lecithin:cholesterol acyltransferase (LCAT) gene. Generation of a new animal model for human LCAT deficiency.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152301

A genetic linkage map of the mouse: current applications and future prospects

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152301

A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152301

High-resolution haplotype structure in the human genome

8 July 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0130101100

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0130101100

A comprehensive genetic map of the mouse genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0130101100

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0130101100

In silico mapping of complex disease-related traits in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0130101100

A comparison of whole-genome shotgun-derived mouse chromosome 16 and the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0130101100

Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0130101100

A genetic map of the mouse with 4,006 simple sequence length polymorphisms

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12612341

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

PCR-amplification of simple sequence repeat variants from pooled DNA samples for rapidly mapping new mutations of the mouse

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12612341

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Automated genotyping using the DNA MassArray technology

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12612341

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0130101100

1 reference

5 August 2017

0 references

1 reference

5 August 2017

1 reference