A DNA segment encoding two genes very tightly linked to Huntington's disease.
about
A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates'The clocks that time us'--circadian rhythms in neurodegenerative disordersComplex patterns of linkage disequilibrium in the Huntington disease region.New mutation to Huntington's disease.Prenatal exclusion testing for Huntington's disease: a problem of too much information.Chromosome jumping from D4S10 (G8) toward the Huntington disease geneConsiderations in using linkage analysis as a presymptomatic test for Huntington's diseaseGenomic imprinting: a possible mechanism for the parental origin effect in Huntington's chorea.Body composition in premanifest Huntington's disease reveals lower bone density compared to controlsRole of oxidative stress and antioxidants in neurodegenerative diseases.The Huntington disease locus is most likely within 325 kilobases of the chromosome 4p telomereCovariate-dependent age-at-onset distributions for Huntington disease.Homozygote for Huntington diseaseDetection of marker associations with a dominant disease gene in genetically complex and heterogeneous diseases.Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus.Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.Improved predictive testing for Huntington disease by using three linked DNA markers.Risk reversals in predictive testing for Huntington disease.The direct screening of cosmid libraries with YAC clones.Clustering of multiallele DNA markers near the Huntington's disease gene.Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4.In vitro amplification techniques for the detection of nucleic acids: new tools for the diagnostic laboratory.MboI RFLP at the D4S43 (C4H) locusSignificant linkage disequilibrium between the Huntington disease gene and the loci D4S10 and D4S95 in the Dutch population.Defined physical limits of the Huntington disease gene candidate region.Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairs.A simple method to detect and estimate heterogeneity: application to Huntington disease, diabetes, and HIV seroconversion.The end in sight for Huntington disease?Predictive testing for Huntington's disease.Huntington's disease: predictive testing and the molecular genetics laboratory.Population-specific genetic modification of Huntington's disease in Venezuela.
P2860
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P2860
A DNA segment encoding two genes very tightly linked to Huntington's disease.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年学术文章
@wuu
1987年学术文章
@zh
1987年学术文章
@zh-cn
1987年学术文章
@zh-hans
1987年学术文章
@zh-my
1987年学术文章
@zh-sg
1987年學術文章
@yue
1987年學術文章
@zh-hant
name
A DNA segment encoding two genes very tightly linked to Huntington's disease.
@en
A DNA segment encoding two genes very tightly linked to Huntington's disease.
@nl
type
label
A DNA segment encoding two genes very tightly linked to Huntington's disease.
@en
A DNA segment encoding two genes very tightly linked to Huntington's disease.
@nl
prefLabel
A DNA segment encoding two genes very tightly linked to Huntington's disease.
@en
A DNA segment encoding two genes very tightly linked to Huntington's disease.
@nl
P2093
P356
P1433
P1476
A DNA segment encoding two genes very tightly linked to Huntington's disease.
@en
P2093
Allitto BA
Gilliam TC
MacDonald ME
P304
P356
10.1126/SCIENCE.2890209
P407
P577
1987-11-01T00:00:00Z