| scholarly article | Q13442814 |
| P50 | author | James F. Gusella | Q1602688 |
| B A Allitto | Q125306018 | ||
| P2093 | author name string | A Poustka | |
| G P Bates | |||
| S Youngman | |||
| M E MacDonald | |||
| D Romano | |||
| Z Sedlacek | |||
| S Baxendale | |||
| W L Whaley | |||
| P2860 | cites work | Genomic sequencing | Q24594942 |
| "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum | Q27860612 | ||
| Identification of a specific telomere terminal transferase activity in Tetrahymena extracts | Q28306745 | ||
| Conservation of the human telomere sequence (TTAGGG)n among vertebrates | Q28776595 | ||
| A highly conserved repetitive DNA sequence, (TTAGGG)n, present at the telomeres of human chromosomes | Q29617061 | ||
| Linkage disequilibrium in Huntington's disease: an improved localisation for the gene | Q33593370 | ||
| Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene | Q33593375 | ||
| Chromosome jumping from D4S10 (G8) toward the Huntington disease gene | Q33644661 | ||
| Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation | Q33837049 | ||
| Yeast artificial chromosomes with 200- to 800-kilobase inserts of human DNA containing HLA, V kappa, 5S, and Xq24-Xq28 sequences. | Q33840781 | ||
| Construction and use of human chromosome jumping libraries from NotI-digested DNA. | Q34162885 | ||
| Mitotic stability of yeast chromosomes: a colony color assay that measures nondisjunction and chromosome loss | Q34197178 | ||
| A polymorphic DNA marker genetically linked to Huntington's disease | Q34255139 | ||
| DNA sequences of telomeres maintained in yeast | Q34255911 | ||
| Cloning human telomeric DNA fragments into Saccharomyces cerevisiae using a yeast-artificial-chromosome vector | Q34297179 | ||
| Homozygotes for Huntington's disease | Q34559291 | ||
| Homozygote for Huntington disease | Q35197558 | ||
| Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus | Q35246016 | ||
| Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90. | Q35247161 | ||
| Isolation and field-inversion gel electrophoresis analysis of DNA markers located close to the Huntington disease gene. | Q35265279 | ||
| Clustering of multiallele DNA markers near the Huntington's disease gene | Q35814879 | ||
| Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4. | Q36080324 | ||
| Removal of repeated sequences from hybridisation probes | Q36138065 | ||
| 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 NotI linking library and isolation of new markers close to the Huntington's disease gene | Q36421909 | ||
| Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment | Q36423793 | ||
| Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors | Q36426834 | ||
| An electrophoretic karyotype for yeast | Q37690127 | ||
| Huntington's disease. Pathogenesis and management | Q39460676 | ||
| Isolation and characterization of a human telomere | Q40452349 | ||
| A DNA probe, D5 [D4S90] mapping to human chromosome 4p16.3. | Q40544675 | ||
| pYAC-RC, a yeast artificial chromosome vector for cloning DNA cut with infrequently cutting restriction endonucleases | Q40554722 | ||
| A computer program package for restriction map analysis and manipulation | Q40559560 | ||
| A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene | Q43611854 | ||
| Separation of large DNA molecules by contour-clamped homogeneous electric fields | Q44137486 | ||
| Recombination events suggest potential sites for the Huntington's disease gene | Q44168431 | ||
| Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere | Q45296842 | ||
| A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease gene | Q45296866 | ||
| Predictive testing for Huntington's disease with use of a linked DNA marker | Q45296919 | ||
| A highly polymorphic locus very tightly linked to the Huntington's disease gene | Q45296953 | ||
| Molecular cloning of human telomeres in yeast. | Q54439350 | ||
| Cloning of human telomeres by complementation in yeast | Q58995576 | ||
| Transformation of yeast spheroplasts without cell fusion | Q68192987 | ||
| Isolation of genomic DNA | Q69405717 | ||
| A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversion | Q69894147 | ||
| Analysis of cosmids using linearization by phage lambda terminase | Q70133853 | ||
| Telomeres: do the ends justify the means? | Q71350297 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Huntington's disease | Q190564 |
| P304 | page(s) | 762-775 | |
| P577 | publication date | 1990-04-01 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene | |
| P478 | volume | 46 |
| Q33806252 | A cloned DNA segment from the telomeric region of human chromosome 4p is not detectably rearranged in Huntington disease patients |
| Q35196100 | A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype |
| Q34142087 | An optimized set of human telomere clones for studying telomere integrity and architecture. |
| Q30501640 | Complex patterns of linkage disequilibrium in the Huntington disease region |
| Q40568126 | Defined physical limits of the Huntington disease gene candidate region |
| Q36236042 | Evidence for the organization of chromatin in megabase pair-sized loops arranged along a random walk path in the human G0/G1 interphase nucleus |
| Q24628626 | Genomic organization and complete sequence of the human gene encoding the beta-subunit of the cGMP phosphodiesterase and its localisation to 4p 16.3 |
| Q36723609 | Identification, characterisation and clinical applications of cosmids from the telomeric and centromeric regions of the long arm of chromosome 22. |
| Q40543368 | Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease region |
| Q33323286 | Isolation and chromosomal localization of a novel nonerythroid ankyrin gene |
| Q28303411 | Isolation, characterization, and localization of human genomic DNA encoding the β1 subunit of the GABAA receptor (GABRB1) |
| Q33597336 | Linkage disequilibrium and recombination make a telomeric site for the Huntington's disease gene unlikely |
| Q35195763 | Minireview: cryptic translocations and telomere integrity |
| Q35195824 | Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome |
| Q33941622 | Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis |
| Q35195406 | Recombination of 4p16 DNA markers in an unusual family with Huntington disease. |
| Q38060615 | Telomere shortening and Alzheimer's disease. |
| Q46971971 | The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease. |
| Q43145917 | The end in sight for Huntington disease? |
| Q33327978 | The role of yeast artificial chromosome clones in generating genome maps |
| Q35888597 | The structure of a subterminal repeated sequence present on many human chromosomes |
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