A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates
about
Evidence for heterogeneity in recombination in the human pseudoautosomal region: high resolution analysis by sperm typing and radiation-hybrid mapping.A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritanceIdentification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4Alpha-fetoprotein related gene (ARG): a new member of the albumin gene family that is no longer functional in primatesA primary linkage map of the porcine genome reveals a low rate of genetic recombinationEvidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1.High-resolution autosomal radiation hybrid maps of the pig genome and their contribution to the genome sequence assembly.Linkage analysis of schizophrenia with five dopamine receptor genes in nine pedigrees.Recombination of 4p16 DNA markers in an unusual family with Huntington disease.The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)Detecting high-resolution polymorphisms in human coding loci by combining PCR and single-strand conformation polymorphism (SSCP) analysis.Influence of aberrant observations on high-resolution linkage analysis outcomesGenetic mapping of the dentinogenesis imperfecta type II locus.Individual variation in recombination among human malesLinkage disequilibrium predicts physical distance in the adenomatous polyposis coli region.Universal mapping probes and the origin of human chromosome 3The map problem: a comparison of genetic and sequence-based physical mapsThe alpha-fetoprotein enhancer region activates the albumin and alpha-fetoprotein promoters during liver developmentOrdering genes: controlling the decision-error probabilitiesIsolation and characterization of new highly polymorphic DNA markers from the Huntington disease region.Linkage disequilibrium patterns vary with chromosomal location: a case study from the von Willebrand factor region.The extent, mechanism, and consequences of genetic variation, for recombination rate
P2860
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P2860
A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates
description
1991 nî lūn-bûn
@nan
1991 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
A detailed multipoint map of h ...... n-specific recombination rates
@ast
A detailed multipoint map of h ...... n-specific recombination rates
@en
A detailed multipoint map of h ...... n-specific recombination rates
@nl
type
label
A detailed multipoint map of h ...... n-specific recombination rates
@ast
A detailed multipoint map of h ...... n-specific recombination rates
@en
A detailed multipoint map of h ...... n-specific recombination rates
@nl
prefLabel
A detailed multipoint map of h ...... n-specific recombination rates
@ast
A detailed multipoint map of h ...... n-specific recombination rates
@en
A detailed multipoint map of h ...... n-specific recombination rates
@nl
P2093
P2860
P1476
A detailed multipoint map of h ...... n-specific recombination rates
@en
P2093
G M Lathrop
J J Wasmuth
K H Buetow
L D Berdahl
N J Leysens
Y Nakamura
P2860
P304
P407
P50
P577
1991-05-01T00:00:00Z