From Wikipedia, the free encyclopedia
Schizophrenia disorder 4, also known as SCZD4, is a human gene.[1]
[edit] References
[edit] Further reading
- Myles-Worsley M, Coon H, McDowell J, et al. (1999). "Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families.". Am. J. Med. Genet. 88 (5): 544-50. PMID 10490714.
- Shaw SH, Kelly M, Smith AB, et al. (1998). "A genome-wide search for schizophrenia susceptibility genes.". Am. J. Med. Genet. 81 (5): 364-76. PMID 9754621.
- Blouin JL, Dombroski BA, Nath SK, et al. (1998). "Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21.". Nat. Genet. 20 (1): 70-3. doi:10.1038/1734. PMID 9731535.
- Pulver AE, Karayiorgou M, Wolyniec PS, et al. (1994). "Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1.". Am. J. Med. Genet. 54 (1): 36-43. doi:10.1002/ajmg.1320540108. PMID 8178837.
- Coon H, Jensen S, Holik J, et al. (1994). "Genomic scan for genes predisposing to schizophrenia.". Am. J. Med. Genet. 54 (1): 59-71. doi:10.1002/ajmg.1320540111. PMID 7909992.
- Lindsay EA, Morris MA, Gos A, et al. (1995). "Schizophrenia and chromosomal deletions within 22q11.2.". Am. J. Hum. Genet. 56 (6): 1502-3. PMID 7762575.
- Karayiorgou M, Morris MA, Morrow B, et al. (1995). "Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.". Proc. Natl. Acad. Sci. U.S.A. 92 (17): 7612-6. PMID 7644464.
- Scambler PJ, Kelly D, Lindsay E, et al. (1992). "Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus.". Lancet 339 (8802): 1138-9. PMID 1349369.
