Genetic mapping: X chromosome
- PMID: 6336311
- DOI: 10.1007/BF00289474
Genetic mapping: X chromosome
Abstract
Starting with the male chiasma distribution for chromosome 2, a significantly better fit is obtained to lod scores for the X chromosome if terminalization of distal chiasmata is assumed. The linkage data are not consistent with a uniform distribution of chiasmata, absence of terminalization, or restriction of terminalization to the distal band. As information about the genetic map of the X chromosome increases, the map will be freed from assumptions about chiasma distribution. At present, however, even fragmentary data on the male are useful to construct a genetic map that, by converting physical assignments to equivalent genetic recombinations, has no inconsistencies between genetic and physical map orders.
Similar articles
-
On the genetic length of the short arm of the human X chromosome.Hum Genet. 1983;65(1):53-5. doi: 10.1007/BF00285028. Hum Genet. 1983. PMID: 6315564 Review.
-
A revised map of chromosome 1.Ann Hum Genet. 1984 Jul;48(3):243-51. doi: 10.1111/j.1469-1809.1984.tb01021.x. Ann Hum Genet. 1984. PMID: 6589974
-
Chiasma-based models of multilocus recombination: increased power for exclusion mapping and gene ordering.Genomics. 1989 Aug;5(2):283-90. doi: 10.1016/0888-7543(89)90059-1. Genomics. 1989. PMID: 2793183
-
A chiasma map of man.Hum Hered. 1977;27(1):38-51. doi: 10.1159/000152850. Hum Hered. 1977. PMID: 844885
-
The topology of meiotic chiasmata prevents terminalization.Ann Hum Genet. 1990 Oct;54(4):307-14. doi: 10.1111/j.1469-1809.1990.tb00386.x. Ann Hum Genet. 1990. PMID: 2285218 Review. No abstract available.
Cited by
-
Assignment of the gene for dyskeratosis congenita to Xq28.Hum Genet. 1986 Apr;72(4):348-51. doi: 10.1007/BF00290963. Hum Genet. 1986. PMID: 3009302
-
The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.Proc Natl Acad Sci U S A. 1985 May;82(9):2824-8. doi: 10.1073/pnas.82.9.2824. Proc Natl Acad Sci U S A. 1985. PMID: 2986139 Free PMC article.
-
On the genetic length of the short arm of the human X chromosome.Hum Genet. 1983;65(1):53-5. doi: 10.1007/BF00285028. Hum Genet. 1983. PMID: 6315564 Review.
-
Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.J Med Genet. 1987 Jan;24(1):14-22. doi: 10.1136/jmg.24.1.14. J Med Genet. 1987. PMID: 2879932 Free PMC article.
-
Incontinentia pigmenti and X-autosome translocations. Non-isotopic in situ hybridization with an X-centromere-specific probe (pSV2X5) reveals a possible X-centromeric breakpoint in one of five published cases.Hum Genet. 1989 Feb;81(3):269-72. doi: 10.1007/BF00279002. Hum Genet. 1989. PMID: 2921037
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Research Materials