References
- ACMG/ASHG. Laboratory guidelines for Huntington Disease Testing. Am. J. Hum. Genet. 1998; 62(5)1243–1247
- Culjkovic B., Stojkovic O., Savic D., Zamurovic N., Nesic M., Major T., Keckarevic D., Zamurovic B., Vukosavic S., Romac S. Comparison of the number of triplets in SCA1, MJD/SCA3, HD, SBMA, DRPLA, MD, FRAXA and FRDA genes in Schizophrenic patients and a healthy population. Am. J. Med. Genet. 2000, in press
- Culjkovic B., Ruzdijic S., Rakic L J., Romac S. Improved plymerase chain reaction conditions for quick diagnosis of Huntington disease. Brain. Res. Prot. 1997; 2: 44–46
- Fisher R. A. Statistical Methods for Research Workers. 12th Ed. Oliver and Boyd, Edinburgh 1954
- Huntington Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable in Huntington's disease chromosomes. Cell 1993; 72: 971–83
- Joo E. J., Lee J. H., Cannon T. D., Price R. A. Possible association between schizophrenia and CAG repeat polymorphism in the spinocerebellar ataxia type 1 (SCA1) gene on human chromosome 6p23. Psychistr. Genet. 1999; 9: 7–11
- Joober R., Benkelfat C., Jannatipour M., Turecki G., Lal S., Mandel J. L., Bloom D., Lalonde P., Lopes-Cendes I., Fortin D., Rouleau G. Polyglutamine-containing proteins in schizophrenia. Mol. Psychiatry 1999; 4: 53–57
- Knapp M., Seuchter S. A., Baur M. P. The haplotype-relative-risk (HRR) method for analysis of association in nuclear families. Am. J. Hum. Genet. 1993; 52: 1085–1093
- Richards R. I., Sutherland G. R. Dynamic mutations: a new class of mutations causing human disease. Cell 1992; 70: 709–12
- Sambrook J., Fritsch E. F., Maniatis T. Molecular Cloning: A Laboratory Manual, 2nd Edition. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY 1989
- SAS STAT. User Guide. SAS Institute, Cary, NC 1991
- Sirugo G., Pakstis A. J., Kidd K. K., Matthysse S., Levy D. L., Holszman P., Breschel T., McInnis M., Ross C. A. Detection of a large CTG/CAG trinucleotide repeat expansion in a schizophrenia kindred. Am. J. Med. Genet. 1997; 74: 546–548