Genetic linkage analysis

Archives of Neurology

Volumn 56, Issue 6, 1999, Pages 667-672

  Pulst, Stefan M ^a,b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ION CHANNEL;

ALZHEIMER DISEASE; ARTICLE; ATAXIA; AUTOSOMAL DOMINANT DISORDER; CHROMOSOMAL LOCALIZATION; CHROMOSOME 1; DEGENERATIVE DISEASE; DISEASE CLASSIFICATION; GENE EXPRESSION; GENE ISOLATION; GENETIC LINKAGE; MARKER GENE; MEIOSIS; PARKINSON DISEASE; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SPINOCEREBELLAR DEGENERATION;

BASE SEQUENCE; CHROMOSOME MAPPING; DINUCLEOTIDE REPEATS; FEMALE; GENETIC DISEASES, INBORN; GENETIC MARKERS; HUMANS; LINKAGE (GENETICS); LINKAGE DISEQUILIBRIUM; MALE; MOLECULAR SEQUENCE DATA; NERVOUS SYSTEM DISEASES; NEURODEGENERATIVE DISEASES; NEUROFIBROMATOSIS 1; NEUROFIBROMATOSIS 2; PEDIGREE;

EID: 0033062050     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.56.6.667     Document Type: Article

References (16)

1. Blumberg RB. Mendel Web Archive. Available at: http://www.netspace.org/MendelWeb/MWpaptoc.html. Accessed November 8, 1998.
2. Bird TD, Ott J, Giblett ER. Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1. Am J Hum Genet. 1982; 34:388-394.
3. Botstein D, White RL, Skolnick M, Davis RW. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am J Hum Genet. 1980;32:314-331.
4. Morton NE. Sequential tests for the detection of linkage. Am J Hum Genet. 1955;7:277-318.
5. Terwiliger J, Ott J. Handbook for Human Genetic Linkage. Baltimore, Md: Johns Hopkins University Press; 1994.
6. Weber JL, May PE. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am J Hum Genet. 1989; 44:388-396.
7. Wang DG, Fan JB, Siao CJ, et al. Large-scale identification, mapping and genotyping of single-nucleotide polymorphisms in the human genome. Science. 1998;280:1077-1082.
8. Dib C, Faure S, Fizames C, et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature. 1996;380:152-154.
9. The Cooperative Human Linkage Center. Available at http://www.chlc.org/ChlcMaps.html. Accessed November 8, 1998.
10. Nystuen A, Benke PJ, Merren J, Stone EM, Sheffield VC. A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman Islands. Hum Mol Genet. 1996;5:525-531.
11. Twist EC, Casaubon LK, Ruttledge MH, et al. Machado Joseph disease maps to the same region of chromosome 14 as the spinocerebellar ataxia type 3 locus. J Med Genet. 1995;32:25-31.
12. Tanzi RE, Blacker D, et al. The genetics of Alzheimer disease: current status and future prospects. Arch Neurol. 1998;55:294-296.
13. Zu L, Grewal R, Figueroa KP, et al. Mapping of a new autosomal dominant ataxia (SCA 10) to chromosome 22. Am J Hum Genet. 1999;64:594-599.
14. Baser ME, Mautner VF, Ragge et al. Presymptomatic diagnosis of neurofibromatosis 2 using linked genetic markers, neuroimaging, and ocular examinations. Neurology. 1996;47:1269-1277.
15. Bell JI, Lathrop GM. Multiple loci for multiple sclerosis. Nat Genet. 1996;13:377-378.
16. Bird TD. Are linkage studies boring? Nat Genet. 1993;4:213-214.