| scholarly article | Q13442814 |
| P50 | author | James F. Gusella | Q1602688 |
| P2093 | author name string | J J Wasmuth | |
| T C Gilliam | |||
| R E Tanzi | |||
| M E MacDonald | |||
| J C Roy | |||
| G D Stewart | |||
| S T Healey | |||
| P2860 | cites work | A highly polymorphic locus in human DNA | Q24608722 |
| "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum | Q27860612 | ||
| CpG-rich islands and the function of DNA methylation | Q28131800 | ||
| Construction of a genetic linkage map in man using restriction fragment length polymorphisms | Q28263594 | ||
| Linkage disequilibrium and evolutionary relationships of DNA variants (restriction enzyme fragment length polymorphisms) at the serum albumin locus | Q28776272 | ||
| Polymorphic DNA region adjacent to the 5' end of the human insulin gene | Q29618325 | ||
| Molecular genetics of human chromosome 4. | Q33672956 | ||
| Precise localization of human beta-globin gene complex on chromosome 11 | Q34038317 | ||
| A polymorphic DNA marker genetically linked to Huntington's disease | Q34255139 | ||
| A strategy to reveal high-frequency RFLPs along the human X chromosome | Q35199942 | ||
| Isolation and localization of DNA segments from specific human chromosomes | Q36389671 | ||
| A cell hybrid and recombinant DNA library that facilitate identification of polymorphic loci in the vicinity of the Huntington disease gene | Q36419339 | ||
| Selective transfer of individual human chromosomes to recipient cells | Q36494354 | ||
| The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers | Q36587060 | ||
| DNA polymorphism and human disease | Q39503970 | ||
| DNA restriction fragment length polymorphisms and heterozygosity in the human genome | Q40140388 | ||
| 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 | ||
| Mapping of the DNA locus D4S10 and the linked Huntington's disease gene to 4p16----p15. | Q45297893 | ||
| DNA Markers for Nervous System Diseases | Q45303524 | ||
| DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man | Q45436146 | ||
| Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker. | Q55060411 | ||
| An estimate of unique DNA sequence heterozygosity in the human genome | Q57264015 | ||
| Localization of cystic fibrosis locus to human chromosome 7cen–q22 | Q57813752 | ||
| A closely linked genetic marker for cystic fibrosis | Q58278151 | ||
| A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16 | Q59066375 | ||
| Report of the Committee on the Genetic Constitution of Chromosomes 3 and 4 | Q69848383 | ||
| Electrophoretic separations of large DNA molecules by periodic inversion of the electric field | Q70022520 | ||
| A test of the role of two oncogenes in inherited predisposition to colon cancer | Q70964520 | ||
| Restriction sites containing CpG show a higher frequency of polymorphism in human DNA | Q72722161 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1445-1458 | |
| P577 | publication date | 1987-02-01 | |
| P1433 | published in | Nucleic Acids Research | Q135122 |
| P1476 | title | Isolation of polymorphic DNA fragments from human chromosome 4. | |
| P478 | volume | 15 |
| Q35247229 | Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction |
| Q33251385 | Characterization and regional mapping of new anonymous chromosome 20-specific DNA markers isolated from a flow-sorted DNA library |
| Q57278706 | Chromosomal deletion 4p15.32→p14 in a treacher collins syndrome patient: Exclusion of the disease locus from and mapping of anonymous DNA sequences to this region |
| Q33644661 | Chromosome jumping from D4S10 (G8) toward the Huntington disease gene |
| Q35814879 | Clustering of multiallele DNA markers near the Huntington's disease gene |
| Q36421909 | Construction of a NotI linking library and isolation of new markers close to the Huntington's disease gene |
| Q34446414 | Construction of gene libraries for each human chromosome |
| Q24619494 | Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia |
| Q70708777 | Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees |
| Q33680461 | Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. |
| Q44654607 | Frequent loss of heterozygosity on chromosomes 16 and 4 in human hepatocellular carcinoma. |
| Q33244565 | Increased recombination adjacent to the Huntington disease-linked D4S10 marker |
| Q33245366 | Isolation and regional localization of a large collection (2,000) of single-copy DNA fragments on human chromosome 3 for mapping and cloning tumor suppressor genes |
| Q36080324 | Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4. |
| Q45936282 | Multiplex genotype determination at a DNA sequence polymorphism cluster in the human immunoglobulin heavy-chain region |
| Q37698525 | Multiplex genotype determination at a large number of gene loci |
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