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Genetic markers and population history: Finland revisitedChromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association studyGenome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern EuropeCould FIV zoonosis responsible of the breakdown of the pathocenosis which has reduced the European CCR5-Delta32 allele frequenciesSearching for Grendel: origin and global spread of the C9ORF72 repeat expansionProportionally more deleterious genetic variation in European than in African populations.ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosisMAOA alters the effects of heavy drinking and childhood physical abuse on risk for severe impulsive acts of violence among alcoholic violent offenders.Two functional variants of the superoxide dismutase genes in Finnish families with asthma.CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease.Accurate Non-parametric Estimation of Recent Effective Population Size from Segments of Identity by Descent.MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies.Subpopulation difference scanning: a strategy for exclusion mapping of susceptibility genes.Exome sequencing in pooled DNA samples to identify maternal pre-eclampsia risk variants.Association of variants in two vitamin e transport genes with circulating vitamin e concentrations and prostate cancer riskSusceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families.Assessment of Parkinson's disease risk loci in GreeceClinical genomics can facilitate countrywide estimation of autosomal recessive disease burden.Replicated evidence for aminoacylase 3 and nephrin gene variations to predict antihypertensive drug responses.Bone marrow failure syndrome caused by homozygous frameshift mutation in the ERCC6L2 gene.Full-gene haplotypes refine CYP2D6 metabolizer phenotype inferences.Association study of 15 novel single-nucleotide polymorphisms of the T-bet locus among Finnish asthma families.An utter refutation of the "fundamental theorem of the HapMap".The language phenotype of a small geographically isolated Russian-speaking population: Implications for genetic and clinical studies of developmental language disorderHaplotype associations define target regions for susceptibility loci in systemic lupus erythematosus
P2860
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P2860
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
name
Human population genetics: lessons from Finland.
@ast
Human population genetics: lessons from Finland.
@en
Human population genetics: lessons from Finland.
@nl
type
label
Human population genetics: lessons from Finland.
@ast
Human population genetics: lessons from Finland.
@en
Human population genetics: lessons from Finland.
@nl
prefLabel
Human population genetics: lessons from Finland.
@ast
Human population genetics: lessons from Finland.
@en
Human population genetics: lessons from Finland.
@nl
P1476
Human population genetics: lessons from Finland.
@en
P304
P356
10.1146/ANNUREV.GENOM.2.1.103
P50
P577
2001-01-01T00:00:00Z