Huntington disease-linked restriction fragment length polymorphism localized within band p16.1 of chromosome 4 by in situ hybridization

scientific article published on September 1986

Huntington disease-linked restriction fragment length polymorphism localized within band p16.1 of chromosome 4 by in situ hybridization is …
instance of (P31):
scholarly articleQ13442814

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P932PMC publication ID1683951
P698PubMed publication ID2876628

P50authorJames F. GusellaQ1602688
P2093author name stringR E Magenis
S Olson
R Sheehy
K Weliky
S Toth-Fejel
G Haight
P2860cites workHuntington disease: genetics and epidemiologyQ24675741
Deficiency on the short arms of a chromosome No. 4Q34241073
Deletion of short arms of chromosome 4?5 in a child with defects of midline fusionQ34241369
A polymorphic DNA marker genetically linked to Huntington's diseaseQ34255139
Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome.Q42507687
Proximal 4p-deletion: phenotype differs from classical 4p-syndromeQ67538013
The human gene map 1 December 1984Q70070782
Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridizationQ70905407
P4510describes a project that usesin situ hybridizationQ2304142
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectHuntington's diseaseQ190564
P304page(s)383-391
P577publication date1986-09-01
P1433published inAmerican Journal of Human GeneticsQ4744249
P1476titleHuntington disease-linked restriction fragment length polymorphism localized within band p16.1 of chromosome 4 by in situ hybridization
P478volume39

Reverse relations

cites work (P2860)
Q35246470A polymorphic DNA marker that represents a conserved expressed sequence in the region of the Huntington disease gene
Q35195719A recombination event that redefines the Huntington disease region
Q36113819An anonymous genomic clone that detects a frequent RFLP adjacent to the D4S10 (G8) marker and Huntington's disease
Q33917989An interspersed repeated sequence specific for human subtelomeric regions
Q33644661Chromosome jumping from D4S10 (G8) toward the Huntington disease gene
Q33681810Considerations in using linkage analysis as a presymptomatic test for Huntington's disease
Q33921449Huntington's disease: pathogenesis, diagnosis and treatment
Q33244565Increased recombination adjacent to the Huntington disease-linked D4S10 marker
Q40543368Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease region
Q35246016Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus
Q36118670Isolation of polymorphic DNA fragments from human chromosome 4.
Q41231153Mapping of the human and mouse bone sialoprotein and osteopontin loci
Q44770705Mouse chromosome 11.
Q35197253The paradigm of Huntington disease

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