Genomic mismatch scanning: a new approach to genetic linkage mapping.
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Yeast microarrays for genome wide parallel genetic and gene expression analysisHaplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autismA maize map standard with sequenced core markers, grass genome reference points and 932 expressed sequence tagged sites (ESTs) in a 1736-locus map.Overview of nucleic acid arrays.Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta.Systematic identification of balanced transposition polymorphisms in Saccharomyces cerevisiaeThe genetics revolution and the assault on rheumatoid arthritis.Phenotypic and genetic analysis of a large family with migraine-associated vertigo.Genetic determinants of human hypertension.Statistical methods for linkage analysis of complex traits from high-resolution maps of identity by descent.An approach for global scanning of single nucleotide variationsDiscovering tumor suppressor genes through genome-wide copy number analysis.High-density arrays and insights into genome function.Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays.PCR candidate region mismatch scanning: adaptation to quantitative, high-throughput genotypingDistribution of genome shared identical by descent by two individuals in grandparent-type relationship.From mutation mapping to phenotype cloning.A resource of mapped human bacterial artificial chromosome clonesMutation detection by mismatch binding protein, MutS, in amplified DNA: application to the cystic fibrosis geneExtended multipoint identity-by-descent analysis of human quantitative traits: efficiency, power, and modeling considerations.Strategies for mapping heterogeneous recessive traits by allele-sharing methodsIdentification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanning.Complex trait mapping in isolated populations: Are specific statistical methods required?Episodic vertical oscillopsia with progressive gait ataxia: clinical description of a new episodic syndrome and evidence of linkage to chromosome 13q.Whole genome analysis: experimental access to all genome sequenced segments through larger-scale efficient oligonucleotide synthesis and PCR.DNA strand exchange and selective DNA annealing promoted by the human immunodeficiency virus type 1 nucleocapsid protein.HLA disease associations: models for the study of complex human genetic disorders.Two-dimensional conformation-dependent electrophoresis (2D-CDE) to separate DNA fragments containing unmatched bulge from complex DNA samplesThe fragile X syndrome: implications of molecular genetics for the clinical syndrome.Analysis of DNA sequences.Trinucleotide repeat instability: genetic features and molecular mechanisms.A general statistical model for detecting complex-trait loci by using affected relative pairs in a genome search2005 Curt Stern Award address. Exploring along a crooked path.Combining information within and between pedigrees for mapping complex traits.The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases I. DNA pooling.Diff-seq: A high throughput sequencing-based mismatch detection assay for DNA variant enrichment and discovery.
P2860
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P2860
Genomic mismatch scanning: a new approach to genetic linkage mapping.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Genomic mismatch scanning: a new approach to genetic linkage mapping.
@en
type
label
Genomic mismatch scanning: a new approach to genetic linkage mapping.
@en
prefLabel
Genomic mismatch scanning: a new approach to genetic linkage mapping.
@en
P2093
P356
P1433
P1476
Genomic mismatch scanning: a new approach to genetic linkage mapping.
@en
P2093
P2888
P356
10.1038/NG0593-11
P407
P577
1993-05-01T00:00:00Z