Assignment of the DIA1 locus to chromosome 22
- PMID: 596823
- DOI: 10.1111/j.1469-1809.1977.tb01909.x
Assignment of the DIA1 locus to chromosome 22
Abstract
Human/rodent hybrid cell cultures were examined for the presence of DIA1 and other marker enzymes. Many of these hybrids were also analysed for human chromosomes. Complete concordance was found only with chromosome 22.
Similar articles
-
Conserved autosomal syntenic group on mouse (MMU) chromosome 15 and human (HSA) chromosome 22: assignment of a gene for arylsulfatase A to MMU 15 and regional mapping of DIA1, ARSA, and ACO2 on HSA 22.Cytogenet Cell Genet. 1981;31(2):58-69. doi: 10.1159/000131626. Cytogenet Cell Genet. 1981. PMID: 6118238
-
Assignment of a human diaphorase (DIA4) to chromosome 16.Ann Hum Genet. 1980 May;43(4):349-53. doi: 10.1111/j.1469-1809.1980.tb01569.x. Ann Hum Genet. 1980. PMID: 6893112
-
Assignment of NADH-cytochrome b5 reductase (DIA1 locus) to human chromosome 22.Hum Genet. 1978 Jun 27;42(3):233-9. doi: 10.1007/BF00291301. Hum Genet. 1978. PMID: 669708
-
Assignment of the gene for NADH diaphorase Dia-1 to Mouse chromosome 15.Somatic Cell Genet. 1980 Nov;6(6):769-76. doi: 10.1007/BF01538975. Somatic Cell Genet. 1980. PMID: 6893763 No abstract available.
-
Terminal 22q deletion associated with a partial deficiency of arylsulphatase A.J Med Genet. 1992 Jun;29(6):432-3. doi: 10.1136/jmg.29.6.432. J Med Genet. 1992. PMID: 1352356 Free PMC article. Review.
Cited by
-
A linkage and physical map of chromosome 22, and some applications to gene mapping.Am J Hum Genet. 1988 Feb;42(2):297-308. Am J Hum Genet. 1988. PMID: 2893546 Free PMC article.
-
Three novel mutations in CYB5R3 gene causing NADH-cytochrome b5 reductase enzyme deficiency leads to recessive congenital methaemoglobinemia.Mol Biol Rep. 2022 Mar;49(3):2141-2147. doi: 10.1007/s11033-021-07031-3. Epub 2022 Jan 22. Mol Biol Rep. 2022. PMID: 35064402
-
Comparative map for mice and humans.Mamm Genome. 1992;3(9):480-536. doi: 10.1007/BF00778825. Mamm Genome. 1992. PMID: 1392257 Review. No abstract available.
-
Gene dosage effect for human triosephosphate isomerase and glyceraldehyde-3-phosphate dehydrogenase in partial trisomy 12p13 and trisomy 18p.Hum Genet. 1978 Nov 24;45(1):63-9. doi: 10.1007/BF00277574. Hum Genet. 1978. PMID: 730182
-
Severe neurological impairment in hereditary methaemoglobinaemia type 2.Eur J Pediatr. 2004 Apr;163(4-5):207-9. doi: 10.1007/s00431-004-1409-x. Epub 2004 Feb 18. Eur J Pediatr. 2004. PMID: 14986124
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous