Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.
Bakker E, et al. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs. Lancet 1: 655-658, 1985. PubMed: 2858615
Greer WL, et al. Linkage relationships of the Wiskott-Aldrich Syndrome to 10 loci in the pericentromeric region of the human X chromosome. Genomics 6: 568-571, 1990. PubMed: 2328995
Wieacker P, et al. Towards a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids. Am. J. Hum. Genet. 36: 265-276, 1984. PubMed: 6324578
Schwartz CE, et al. Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21. Am. J. Hum. Genet. 47: 454-458, 1990. PubMed: 2393020
Thakker RV, et al. Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families. Genomics 8: 189-193, 1990. PubMed: 1979046
Musarella MA, et al. Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3. Genomics 5: 727-737, 1989. PubMed: 2574143
Derom C, et al. Zygosity determination in newborn twins using DNA variants. J. Med. Genet. 22: 279-282, 1985. PubMed: 2995674
Skolnick MH, Francke U. Report of the committee on human gene mapping by recombinant DNA techniques. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. Cytogenet. Cell Genet. 32: 194-204, 1982. PubMed: 7140362
European Society of Human Genetics. Abstracts from symposium on 'X- linked diseases'. Madrid, Spain, September 29-October 2, 1982. Clin. Genet. 23: 195-259, 1983. PubMed: 6682728
Peacocke M, Siminovitch KA. Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome. Proc. Natl. Acad. Sci. USA 84: 3430-3433, 1987. PubMed: 3472214
