Where is the gene for GALT?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00279064.pdf
Reference15 articles.
1. Allerdice, P. W., Tedesco, T. A.: Localization of human gene for galactose-1-phosphate uridyltransferase. Lancet 1975 II, 39
2. Beutler, E., Baluda, M. C.: Improved method for measuring galactose-1-P uridyl transferase activity of erythrocytes. Clin. Chim. Acta 13, 369?379 (1966)
3. Funderburk, S. J., Sparkes, R. S., Klisak, I.: The 9p-syndrome. J. Med. Genet. 16, 75?79 (1979)
4. Kondo, I., Hirano, T., Hamaguchi, H., Ohta, Y., Haibara, S., Nakai, H., Takita, H.: A case of trisomy 3q21?qter syndrome. Hum. Genet. 46, 141?147 (1979)
5. Meera Khan, P., Wijnen, L. M. M., Pearson, P. L.: Assignment of a human galactose-1-phosphate uridyltransferase gene (GALT) to chromosome 9 in human-Chinese hamster somatic cell hybrids. Cytogenet. Cell Genet. 22, 207?211 (1978)
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1. Length of the chromosomal segment marked by galactose-1-phosphate uridyl transferase and soluble aconitase and conserved since divergence of lineages leading to mouse and man;Genetical Research;1988-10
2. Conserved linkage of soluble aconitase and galactose-1-phosphate uridyl transferase in mouse and man: assignment of these genes to mouse chromosome 4;Cytogenetic and Genome Research;1982
3. The contribution of chromosome aberrations to the precision of human gene mapping;Cytogenetic and Genome Research;1982
4. Expression of GALT in two unrelated 9p- patients. Evidence for assignment of the GALT locus to the 9p21 band;Human Genetics;1981-11
5. Familial insertional translocation of a portion of 3q into 11q resulting in duplication and deletion of region 3q22.1→q24 in different offspring;American Journal of Medical Genetics;1981
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