scholarly article | Q13442814 |
P50 | author | James F. Gusella | Q1602688 |
P2093 | author name string | R E Magenis | |
S Olson | |||
R Sheehy | |||
K Weliky | |||
S Toth-Fejel | |||
G Haight | |||
P2860 | cites work | Huntington disease: genetics and epidemiology | Q24675741 |
Deficiency on the short arms of a chromosome No. 4 | Q34241073 | ||
Deletion of short arms of chromosome 4?5 in a child with defects of midline fusion | Q34241369 | ||
A polymorphic DNA marker genetically linked to Huntington's disease | Q34255139 | ||
Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome. | Q42507687 | ||
Proximal 4p-deletion: phenotype differs from classical 4p-syndrome | Q67538013 | ||
The human gene map 1 December 1984 | Q70070782 | ||
Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization | Q70905407 | ||
P4510 | describes a project that uses | in situ hybridization | Q2304142 |
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Huntington's disease | Q190564 |
P304 | page(s) | 383-391 | |
P577 | publication date | 1986-09-01 | |
P1433 | published in | American Journal of Human Genetics | Q4744249 |
P1476 | title | Huntington disease-linked restriction fragment length polymorphism localized within band p16.1 of chromosome 4 by in situ hybridization | |
P478 | volume | 39 |
Q35246470 | A polymorphic DNA marker that represents a conserved expressed sequence in the region of the Huntington disease gene |
Q35195719 | A recombination event that redefines the Huntington disease region |
Q36113819 | An anonymous genomic clone that detects a frequent RFLP adjacent to the D4S10 (G8) marker and Huntington's disease |
Q33917989 | An interspersed repeated sequence specific for human subtelomeric regions |
Q33644661 | Chromosome jumping from D4S10 (G8) toward the Huntington disease gene |
Q33681810 | Considerations in using linkage analysis as a presymptomatic test for Huntington's disease |
Q33921449 | Huntington's disease: pathogenesis, diagnosis and treatment |
Q33244565 | Increased recombination adjacent to the Huntington disease-linked D4S10 marker |
Q40543368 | Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease region |
Q35246016 | Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus |
Q36118670 | Isolation of polymorphic DNA fragments from human chromosome 4. |
Q41231153 | Mapping of the human and mouse bone sialoprotein and osteopontin loci |
Q44770705 | Mouse chromosome 11. |
Q35197253 | The paradigm of Huntington disease |
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