| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1053629396 |
| P356 | DOI | 10.1007/BF00357002 |
| P698 | PubMed publication ID | 7919654 |
| P50 | author | James F. Gusella | Q1602688 |
| P2093 | author name string | M E MacDonald | |
| C M Ambrose | |||
| M P Duyao | |||
| S Roffler-Tarlov | |||
| C L Grosson | |||
| P2860 | cites work | A gene from chromosome 4p16.3 with similarity to a superfamily of transporter proteins | Q24311710 |
| Cloning, molecular characterization, and chromosomal assignment of a gene encoding a second D1 dopamine receptor subtype: differential expression pattern in rat brain compared with the D1A receptor | Q24321094 | ||
| A novel G protein-coupled receptor kinase gene cloned from 4p16.3 | Q24337701 | ||
| Multiple human D5 dopamine receptor genes: a functional receptor and two pseudogenes | Q24560472 | ||
| Genomic organization and complete sequence of the human gene encoding the beta-subunit of the cGMP phosphodiesterase and its localisation to 4p 16.3 | Q24628626 | ||
| "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum | Q27860612 | ||
| A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. | Q27860836 | ||
| Cloning of the alpha-adducin gene from the Huntington's disease candidate region of chromosome 4 by exon amplification | Q28118724 | ||
| Chromosome mapping of the rod photoreceptor cGMP phosphodiesterase beta-subunit gene in mouse and human: tight linkage to the Huntington disease region (4p16.3) | Q28210084 | ||
| Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate region | Q31158475 | ||
| Genetic analysis of the dominant white-spotting (W) region on mouse chromosome 5: identification of cloned DNA markers near W. | Q33686776 | ||
| Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation | Q33837049 | ||
| A polymorphic DNA marker genetically linked to Huntington's disease | Q34255139 | ||
| Homozygotes for Huntington's disease | Q34559291 | ||
| Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome | Q35195824 | ||
| Homozygote for Huntington disease | Q35197558 | ||
| Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4 | Q35225332 | ||
| A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene | Q36766598 | ||
| Huntington's disease. Pathogenesis and management | Q39460676 | ||
| New DNA markers in the Huntington's disease gene candidate region | Q41667937 | ||
| Huntington disease-linked locus D4S111 exposed as the alpha-L-iduronidase gene. | Q41677044 | ||
| The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene | Q44659531 | ||
| Synteny on mouse chromosome 5 of homologs for human DNA loci linked to the Huntington disease gene | Q44889876 | ||
| The murine Il-6 gene maps to the proximal region of chromosome 5. | Q45266952 | ||
| Hunting for Huntington's disease. | Q45290188 | ||
| Delineation of a 50 kilobase DNA segment containing the recombination site in a sporadic case of Huntington's disease | Q45291097 | ||
| Linkage, but not gene order, of homologous loci, including alpha-L-iduronidase (Idua), is conserved in the Huntington disease region of the mouse and human genomes. | Q45292058 | ||
| A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4. | Q45292433 | ||
| Physical and genetic localization of quinonoid dihydropteridine reductase gene (QDPR) on short arm of chromosome 4. | Q45296863 | ||
| 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 | ||
| Mapping of the two mouse engrailed-like genes: close linkage of En-1 to dominant hemimelia (Dh) on chromosome 1 and of En-2 to hemimelic extra-toes (Hx) on chromosome 5. | Q46353237 | ||
| En-1 and En-2, two mouse genes with sequence homology to the Drosophila engrailed gene: expression during embryogenesis | Q46494637 | ||
| Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 5 | Q72676072 | ||
| P433 | issue | 7 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Huntington's disease | Q190564 |
| P1104 | number of pages | 5 | |
| P304 | page(s) | 424-428 | |
| P577 | publication date | 1994-07-01 | |
| P1433 | published in | Mammalian Genome | Q1348949 |
| P1476 | title | Synteny conservation of the Huntington's disease gene and surrounding loci on mouse Chromosome 5. | |
| P478 | volume | 5 |
| Q45307541 | Comparative sequence analysis of the human and pufferfish Huntington's disease genes |
| Q35367599 | Glycosaminoglycan storage disorders: a review |
| Q41072019 | Molecular cloning, chromosomal mapping and developmental expression of BAPX1, a novel human homeobox-containing gene homologous to Drosophila bagpipe |
| Q37714529 | Pufferfish and new paradigm for comparative genome analysis |
| Q28145383 | The GRK4 subfamily of G protein-coupled receptor kinases. Alternative splicing, gene organization, and sequence conservation |
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