Integrating maps of chromosome 16
- PMID: 8353417
- DOI: 10.1016/0959-437x(93)90116-7
Integrating maps of chromosome 16
Abstract
The recently published, detailed cytogenetic-based physical map of chromosome 16 has the highest resolution of any autosomal cytogenetic map thus far constructed. The genetic map has been integrated with the cytogenetic map to facilitate the regional localization of disease genes by linkage. Disease genes for tuberous sclerosis, familial Mediterranean fever, Rubinstein-Taybi syndrome and Morquio A syndrome have now been assigned to chromosome 16. The search for the adult polycystic kidney disease gene has recently been narrowed to the analysis of candidate loci on chromosome 16, and localization of the gene determining juvenile Batten disease has been further refined by disequilibrium mapping.
Similar articles
-
Integration of the cytogenetic and genetic linkage maps of human chromosome 16 using 50 physical intervals and 50 polymorphic loci.Cytogenet Cell Genet. 1993;62(4):194-8. doi: 10.1159/000133474. Cytogenet Cell Genet. 1993. PMID: 8440136
-
Rubinstein-Taybi syndrome and familial Mediterranean fever in a single patient: two distinct genetic diseases located on chromosome 16p13.3.J Natl Med Assoc. 2006 Oct;98(10):1692-3. J Natl Med Assoc. 2006. PMID: 17052063 Free PMC article.
-
Fine genetic mapping of the Batten disease locus (CLN3) by haplotype analysis and demonstration of allelic association with chromosome 16p microsatellite loci.Genomics. 1993 May;16(2):455-60. doi: 10.1006/geno.1993.1210. Genomics. 1993. PMID: 8314582
-
Mapping the locus of autosomal dominant polycystic kidney disease: diagnostic application.Clin Chem. 1989 Jul;35(7 Suppl):B13-6. Clin Chem. 1989. PMID: 2568192 Review.
-
Tentative assignment of a locus for Rubinstein-Taybi syndrome to 16p13.3 by a de novo reciprocal translocation, t(7;16)(q34;p13.3).Am J Med Genet. 1992 Sep 15;44(2):237-41. doi: 10.1002/ajmg.1320440223. Am J Med Genet. 1992. PMID: 1456298 Review.
Cited by
-
The gene coding for the B cell surface protein CD19 is localized on human chromosome 16p11.Hum Genet. 1995 Feb;95(2):223-5. doi: 10.1007/BF00209407. Hum Genet. 1995. PMID: 7532151
-
Gene expression profiling of lymphoblastoid cell lines from monozygotic twins discordant in severity of autism reveals differential regulation of neurologically relevant genes.BMC Genomics. 2006 May 18;7:118. doi: 10.1186/1471-2164-7-118. BMC Genomics. 2006. PMID: 16709250 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources