scholarly article | Q13442814 |
P356 | DOI | 10.1139/G97-010 |
P698 | PubMed publication ID | 9061915 |
P2093 | author name string | S Wood | |
M Schertzer | |||
R Bruskiewich | |||
P2860 | cites work | Basic local alignment search tool | Q25938991 |
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity | Q26778490 | ||
Colony hybridization: a method for the isolation of cloned DNAs that contain a specific gene | Q28142488 | ||
Structure and transcriptional regulation of protein phosphatase 2A catalytic subunit genes | Q28279310 | ||
A hybrid cell mapping panel for regional localization of probes to human chromosome 8 | Q28281719 | ||
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Mapping the whole human genome by fingerprinting yeast artificial chromosomes | Q31095563 | ||
Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources | Q34301388 | ||
Integrated mapping analysis of the Werner syndrome region of chromosome 8. | Q34316597 | ||
Genetic linkage of Werner's syndrome to five markers on chromosome 8 | Q34616225 | ||
Construction of yeast artificial chromosome libraries with large inserts using fractionation by pulsed-field gel electrophoresis | Q35225775 | ||
An improved method for the screening of YAC libraries | Q35874033 | ||
Genetic association between chromosome 8 microsatellite (MS8-134) and Werner syndrome (WRN): chromosome microdissection and homozygosity mapping | Q36671409 | ||
A first-generation physical map of the human genome | Q36757666 | ||
A panel of radiation hybrids for human chromosome 8. | Q41470225 | ||
Generation of novel sequence tagged sites (STSs) from discrete chromosomal regions using Alu-PCR. | Q44385949 | ||
A genetic analysis of the Werner syndrome region on human chromosome 8p. | Q46934105 | ||
A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process | Q55953422 | ||
Integrated Map of the Chromosome 8p12–p21 Region, a Region Involved in Human Cancers and Werner Syndrome | Q58062339 | ||
P433 | issue | 1 | |
P921 | main subject | Werner syndrome | Q1154619 |
P304 | page(s) | 77-83 | |
P577 | publication date | 1997-02-01 | |
P1433 | published in | Genome | Q15765118 |
P1476 | title | A 2.8 megabase YAC contig spanning D8S339, which is tightly linked to the Werner syndrome locus | |
P478 | volume | 40 |
Q24679438 | Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility | cites work | P2860 |
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