2008, Number 6
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Gac Med Mex 2008; 144 (6)
Genómica y esquizofrenia
Salamanca-Gómez F
Language: Spanish
References: 7
Page: 547-548
PDF size: 28.00 Kb.
Text Extraction
No abstract
REFERENCES
Sherrington R, Brynjolfsson J, Petturson H, Potter M, Duddleston K, Barraclough B, et al. Localization of a susceptibility locus for schizophrenia on chromosome 5. Nature 1988;336:164-167.
Wang S, Sun C, Walczak C, Ziegle JS, Kipps BR, Goldin LR, et al. Evidence for a susceptibility locus for schizophrenia on cromosome 6 pter-p22. Nature Genet 1995;10:41-46.
Karayiorgou M, Morris A, Morrow B, Shprintzen RJ, Goldberg R, Borrow J, et al. Schizoprenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc Natl Acad Sci USA 1995;92:7612-7616.
Brzustowics LM, Hodgkinson KA, Chow EW, Honer WG, Bassett AS. Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22. Science 2000;288:678-682.
Gurling HM, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo BS, et al. Genome wide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia on chromosoma 1q21.2, 5q33.2, and 8q21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23. Am J Hum Genet 2001;68:661-673.
Stefansson H, Rujescu D, Cichon S, Pietilainen OPH, Ingason A, Steinberg S, et al. Large recurrent microdeletions associated with schizophrenia. Nature 2008;445:232-236.
The International Schizophrenia Consortium. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 2008;455:237-241.