About: Common deletions and SNPs are in linkage disequilibrium in the human genome

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About: Common deletions and SNPs are in linkage disequilibrium in the human genome Goto Sponge NotDistinct Permalink

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scientific article published on 04 December 2005

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2005 (fr) наукова стаття, опублікована в грудні 2005 (uk) im Dezember 2005 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 2005 (ast) scientific article published on 04 December 2005 (en)
publication date	wds:Q57264082-7C21D0FE-BAAD-4C61-9891-18AB690E3653
publication date	2005-12-04 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57264082-B6619191-C696-4194-9608-0307332E5D15
language of work or name	English
exact match	wds:Q57264082-F3BDE22E-B2BB-4225-803F-4D6976FC343D
exact match	https://scigraph.springernature.com/pub.10.1038/ng1695
cites work	wds:Q57264082-0659A29B-BB92-4D6F-AC8E-38738A9101EA wds:Q57264082-12C99B0E-2AC1-413C-8AA6-B951971389EC wds:Q57264082-198952B7-68B9-42A8-93E4-4B60686A8B30 wds:Q57264082-23911ACC-FE5B-4936-9801-9955DF8297B1 wds:Q57264082-2990BC6A-6539-4D41-8846-4B3F8188BD49 wds:Q57264082-5790245E-1112-4FAF-953F-7382D2894E0F wds:Q57264082-598C7050-9F41-42C1-9E0D-AA13815B593B wds:Q57264082-5B30D6AF-2400-466B-AA12-ACF5150BD627 wds:Q57264082-5FB910B0-E57F-4E60-9E53-A9174D304807 wds:Q57264082-63D021A3-4267-41A2-993E-64F8F1432BAE wds:Q57264082-6F2070C5-3347-4B16-B060-65F600BAD980 wds:Q57264082-711F2DFB-77FE-4466-8906-10368960193E wds:Q57264082-7234E45B-E76B-4136-8F5E-361A3F736F71 wds:Q57264082-8507925D-9DAD-4B4B-9147-0BA86325192F wds:Q57264082-8FBF2713-A101-4E34-87D7-4D311EF55091 wds:Q57264082-90E23635-F6A7-447C-8C97-D0F42833D355 wds:Q57264082-AA21BE28-1558-438E-97FD-D7DBA2A0B9FB wds:Q57264082-C78449A9-369D-4B71-8A16-960666EF67D0 wds:Q57264082-C9329FC1-8DCD-4B06-AD9A-45AEA6D3A14E wds:Q57264082-C9CF824F-C615-4C2C-AD39-9B68749F10E7 wds:Q57264082-CB7C4964-7341-4FE8-84F5-2A2BB2AAFCA0 wds:Q57264082-D5BC8EBC-214A-455B-AB54-15A922BBB8AB wds:Q57264082-DDB2900A-EDF3-42FA-96B9-596B463FE773 wds:Q57264082-E0446F71-2067-4010-BCD6-1E211E1F611A wds:Q57264082-E66845DE-60DC-4466-A5C2-2D89E6549C28 wds:Q57264082-EE8C158D-3334-413D-86DF-0DEA3BC5BCF2 wds:Q57264082-EF7279D0-F5C3-4142-8281-1893F7B9F2F0
cites work	The chromosomal arrangement of human alpha-like globin genes: sequence homology and alpha-globin gene deletions. Fine-scale structural variation of the human genome Recent segmental duplications in the human genome Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates Detection of large-scale variation in the human genome Characterization of single-nucleotide polymorphisms in coding regions of human genes Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis Large-scale copy number polymorphism in the human genome Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes Common deletion polymorphisms in the human genome. A high-resolution survey of deletion polymorphism in the human genome alpha-Synuclein locus triplication causes Parkinson's disease Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Prevalence of 22q11 microdeletion Segmental duplications and copy-number variation in the human genome The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility A common inversion under selection in Europeans Whole-genome patterns of common DNA variation in three human populations Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1 Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome A population study of chromosome 22q11 deletions in infancy Molecular mechanisms for genomic disorders A novel α-globin gene arrangement in man Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study Frequency and predictive value of 22q11 deletion
author name string	wds:Q57264082-667FF902-2948-4664-9393-40AFB15AE41F wds:Q57264082-A17FD3CC-1F8C-475A-AFDB-20D9CEB3F6E5 wds:Q57264082-E8FFC5B1-E3B7-45FE-AAAC-074EDB6A0D36
author name string	Andrew P Kloek Michael Jen Xiyin Chen
rdfs:label	Common deletions and SNPs are in linkage disequilibrium in the human genome (en) Common deletions and SNPs are in linkage disequilibrium in the human genome (nl)
skos:prefLabel	Common deletions and SNPs are in linkage disequilibrium in the human genome (en) Common deletions and SNPs are in linkage disequilibrium in the human genome (nl)
name	Common deletions and SNPs are in linkage disequilibrium in the human genome (en) Common deletions and SNPs are in linkage disequilibrium in the human genome (nl)
author	wds:Q57264082-6CB096B8-0B1F-446C-A67E-EA810B522ED7 wds:Q57264082-8EFA4089-8E48-4DE1-BF11-7530021AC9D6
author	Kelly A. Frazer David A Hinds
title	wds:Q57264082-1CC9857A-75C6-47D5-9F44-18F21F4D7040
title	Common deletions and SNPs are in linkage disequilibrium in the human genome (en)
page(s)	wds:Q57264082-23FE170D-18B0-4208-BC6B-BBAA23F06DFB
page(s)	82-85
instance of	wds:Q57264082-5A76E405-A200-4932-A30E-35751DD9F291
instance of	scholarly article
main subject	wds:Q57264082-76C15EFE-EE6E-4999-8689-08D281193919 wds:Q57264082-7A813685-52DD-4965-82A9-CAECB8D0DBFF
main subject	disequilibrium linkage disequilibrium
PubMed ID	wds:Q57264082-FB5210AB-F1FA-4980-BB31-D944862F1C64
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16327809
PubMed ID	16327809
published in	wds:Q57264082-FFE7A81F-71CC-43CB-84FE-F69F533DC9CD
published in	Nature Genetics
issue	wds:Q57264082-1E3B6242-7B0C-4EC3-A4B9-5DDB4FF60B6D
volume	wds:Q57264082-F1AFBB3E-170A-432E-82C2-FE4E43F07C4D

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