scholarly article | Q13442814 |
P819 | ADS bibcode | 1988PNAS...85.6437R |
P356 | DOI | 10.1073/PNAS.85.17.6437 |
P932 | PMC publication ID | 281987 |
P698 | PubMed publication ID | 2901098 |
P5875 | ResearchGate publication ID | 20255357 |
P50 | author | James F. Gusella | Q1602688 |
Francis Collins | Q336658 | ||
P2093 | author name string | J J Wasmuth | |
T C Gilliam | |||
J E Richards | |||
M L Drumm | |||
J L Cole | |||
P2860 | cites work | Electrophoretic separations of large DNA molecules by periodic inversion of the electric field | Q70022520 |
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Directional cloning of DNA fragments at a large distance from an initial probe: a circularization method | Q34245481 | ||
A polymorphic DNA marker genetically linked to Huntington's disease | Q34255139 | ||
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The William Allan Memorial Award address: Reverse genetics and beyond | Q35200050 | ||
Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus | Q35246016 | ||
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Isolation of polymorphic DNA fragments from human chromosome 4. | Q36118670 | ||
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A cell hybrid and recombinant DNA library that facilitate identification of polymorphic loci in the vicinity of the Huntington disease gene | Q36419339 | ||
Construction of a general human chromosome jumping library, with application to cystic fibrosis | Q36419775 | ||
Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors | Q36426834 | ||
Derivation of clones close to met by preparative field inversion gel electrophoresis | Q36427000 | ||
A cosmid vector that facilitates restriction enzyme mapping | Q37687782 | ||
Reverse genetics and human disease | Q38168782 | ||
Huntington's disease. Pathogenesis and management | Q39460676 | ||
Huntington disease-linked restriction fragment length polymorphism localized within band p16.1 of chromosome 4 by in situ hybridization | Q40592141 | ||
Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome. | Q42507687 | ||
Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere | Q45296842 | ||
A DNA segment encoding two genes very tightly linked to Huntington's disease | Q45296882 | ||
A highly polymorphic locus very tightly linked to the Huntington's disease gene | Q45296953 | ||
Further studies on bivalent chiasma frequency in human males with normal karyotypes. | Q52666209 | ||
Strategies for mapping and cloning macroregions of mammalian genomes | Q69817237 | ||
P433 | issue | 17 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Huntington's disease | Q190564 |
P304 | page(s) | 6437-6441 | |
P577 | publication date | 1988-09-01 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Chromosome jumping from D4S10 (G8) toward the Huntington disease gene | |
P478 | volume | 85 |
Q33963473 | A chromosome jump crosses a translocation breakpoint in the von Recklinghausen neurofibromatosis region |
Q36766598 | A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene |
Q24679121 | A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates |
Q33839565 | A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene |
Q45288997 | Allele frequencies and linkage disequilibrium of polymorphic DNA markers of the Huntington disease region in the German population |
Q31158475 | Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate region |
Q34307943 | Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia |
Q40568126 | Defined physical limits of the Huntington disease gene candidate region |
Q33494932 | Derivation of clones from the choroideremia locus by preparative field inversion gel electrophoresis |
Q35247161 | Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90. |
Q45298333 | History of genetic disease: the molecular genetics of Huntington disease - a history |
Q35197620 | Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus |
Q36627108 | Incorporating genomics into the toolkit of nematology |
Q35555012 | Isolation of additional polymorphic clones from the cystic fibrosis region, using chromosome jumping from D7S8. |
Q33294055 | Laser microdissection and single unique primer PCR allow generation of regional chromosome DNA clones from a single human chromosome |
Q58999421 | Moving in on plant genes |
Q35243890 | New insights into the clinical features, pathogenesis and molecular genetics of Huntington disease |
Q45290868 | Prenatal diagnosis of Huntington's disease (HD): Experiences with six cases and PCR |
Q44228164 | Presymptomatic, prenatal, and exclusion testing for Huntington disease using seven closely linked DNA markers |
Q37356324 | Role of in silico tools in gene discovery |
Q40553360 | Significant linkage disequilibrium between the Huntington disease gene and the loci D4S10 and D4S95 in the Dutch population |
Q45293418 | Site-Specific Cleavage of Human Chromosome 4 Mediated by Triple-Helix Formation |
Q34326319 | The Huntington disease locus is most likely within 325 kilobases of the chromosome 4p telomere |
Q43145917 | The end in sight for Huntington disease? |
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