about
A genomewide screen of 345 families for autism-susceptibility loci.Novel vitiligo susceptibility loci on chromosomes 7 (AIS2) and 8 (AIS3), confirmation of SLEV1 on chromosome 17, and their roles in an autoimmune diathesisGenomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26.G2D: a tool for mining genes associated with disease.Genetics of type 1 diabetes mellitusLinkage and association studies in African- and Caucasian-American populations demonstrate that SHC3 is a novel susceptibility locus for nicotine dependenceGenome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's diseaseHorn type and horn length genes map to the same chromosomal region in Soay sheepGenetic susceptibility to tuberculosis.A genomewide search finds major susceptibility loci for nicotine dependence on chromosome 10 in African Americans.Genome-wide linkage scan for nicotine dependence in European Americans and its converging results with African Americans in the Mid-South Tobacco Family sample.A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study.A genome-wide scan to identify loci for smoking rate in the Framingham Heart Study population.Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease.Complex aetiology of an apparently Mendelian form of mental retardation.A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11A genomewide screen for generalized vitiligo: confirmation of AIS1 on chromosome 1p31 and evidence for additional susceptibility lociCombined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16qAttention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.Intracranial aneurysms in Finnish families: confirmation of linkage and refinement of the interval to chromosome 19q13.3.A novel linkage to generalized vitiligo on 4q13-q21 identified in a genomewide linkage analysis of Chinese families.The Ising model in physics and statistical genetics.Genomewide significant linkage to migrainous headache on chromosome 5q21.A genomewide screen for autism susceptibility loci.A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1qA genomewide scan for type 1-diabetes susceptibility in Scandinavian families: identification of new loci with evidence of interactions.Statistical approaches to gene mappingClass II cytokine receptor gene cluster is a major locus for hepatitis B persistenceFurther genetic evidence for a panic disorder syndrome mapping to chromosome 13q.Genetic architecture of purple pigmentation and tagging of some loci to SSR markers in pearl millet, Pennisetum glaucum (L.) R. Br.Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family.Replicated analysis of the genetic architecture of quantitative traits in two wild great tit populations.Bivariate linkage study of proximal hip geometry and body size indices: the Framingham study.Major Loci on Chromosomes 8q and 3q Control Interferon γ Production Triggered by Bacillus Calmette-Guerin and 6-kDa Early Secretory Antigen Target, Respectively, in Various Populations.The genetic architecture of sexually selected traits in two natural populations of Drosophila montana.The fibromyalgia family study: a genome-wide linkage scan study.A genome wide linkage scan of metacarpal size and geometry in the Framingham StudyMicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: functional and therapeutic implications for gene expression and the pathogenesis of hypertension.Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism.Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk Island.
P2860
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P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
All LODs are not created equal.
@ast
All LODs are not created equal.
@en
type
label
All LODs are not created equal.
@ast
All LODs are not created equal.
@en
prefLabel
All LODs are not created equal.
@ast
All LODs are not created equal.
@en
P2860
P356
P1476
All LODs are not created equal.
@en
P2093
D R Nyholt
P2860
P304
P356
10.1086/303029
P407
P577
2000-07-06T00:00:00Z