References
- Anand R., Villosante A., Tyler-Smith C. Construction of yeast artificial chromosome libraries with large inserts using fractionation of pulsed field gel electrophoresis. Nucleic Acids Research 1989; 17: 3425–3431
- Bird A. P. CpG-rich islands and the function of DNA methylation. Nature 1986; 12: 209–213
- Chamberlain S., Shaw J., Rowland A., Wallis J., South S., Nakamura Y., Von Gabain A., Farrall M., Williamson R. Mapping of mutation causing Friedreich's ataxia to human chromosome 9. Nature 1988; 334: 248–250
- Cohen M. L., Golde T. E., Usiak M. F., Younkin L. H., Younkin S. G. In situ hybridisation of nucleus basalis neurons shows increased Bamyloid mRNA in Alzheimer's disease. 1988; 1227–1231, Proceedings of the National Academy of SciencesUSA85
- Daiger S. P., Lidsky A. S., Chakraborty R., Koch R., Guttler F., Woo S. L. C. Polymorphic DNA haplotypes at the phenylalanine locus in prenatal diagnosis of phenylketonuria. Lancet 1986; 1: 229–231
- Dilella A. G., Morvit J., Brayton K., Woo S. L. C. An amino acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2. Nature 1987; 327: 333–336
- Gusela J. F., Wexler N. S., Conneally P. M., Naylor S. L. A polymorphic DNA marker genetically linked in Huntington's disease. Nature 1983; 306: 234–238
- Gusela J. F., Tanzi R. E., Anderson M. A., Hobbs W. DNA markers for nervous system disease. Science 1984; 225: 1320–1326, et al.
- Higgins G. A., Lewis D. A., Bahmanyar S., Goldgarber D., Gajdusek D. C., Morrison J. H., Wilson M. C. Differential regulation of amyloid B protein mRNA expression within hippocampal neuronal sub-population in Alzheimer's disease. 1988; 1292–1301, Proceedings of the National Academy of Sciences, USA, 85
- Kendler K. S., Eaves L. J. Models for the joint effect of genotype and environment on liability to psychiatric illness. American Journal of Psychiatry 1986; 143: 279–289
- Kimura M. The neutral theory of molecular evolution. Scientific American 1979; 241: 98–100
- Monaco A. P., Bertelson C. J., Middlesworth W., Colletti C. A. Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment. Nature 1985; 316: 842–845, et al.: (
- Monaco A. P., Neve R. L., Colletti-Feeno C., Bertelson C. J. Isolation of candidate cDNAs for portions of the Duchenne nuscular dystrophy gene. Nature 1986; 323: 646–650, et al.: (
- Owen M. J., Whatley S. A. Polymorphic DNA markers and mental disease. Psychological Medicine 1988; 18: 529–533
- Poustka A., Pohl T., Barlow D. P., Zehetner G., Craig A., Michiels F., Ehrich E., Frischauf A. M., Lehrach H. Molecular approaches to mammalian genetics. Cold Spring Harbour Symposia of Quantitative Biology 1986; 51: 131–139, part 1
- Smith C. L., Klco G. R., Cantor C. R. Pulsed-field gel electrophoresia and the technology of large DNS molecules. Genome Analysis: a practical approach, K. E. Davies. IRL press, Oxford 1988; 41–72
- Steel C. M. DNA in medicine: The tools. Pan I. Lancet 1984a; 908–911, ii
- Steel C. M. DNA in medicine: The tools. Pan II. Lancet 1984b; 966–968, ii
- Weatherall D. J. The New Genetics and Clinical Practice 2nd edn. Oxford University Press, Oxford 1985
- Whatley S. A., Owen M. J., Murray R. M. The new genetics and neuropsychiatric disorders. The Bridge Between Neurology and Psychiatry, E. H. Reynolds, M. R. Trimble. Churchill Livingstone, Edinburgh 1989; 353–379
- Woo S. L. C., Lidsky A. S., Guttler F., Chandra T., Robson K. J. H. Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical pheylketonuria. Nature 1983; 306: 151–155