The principles of human biochemical genetics / Harry Harris.

  • Harry Harris
Date:
1975
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Licence: Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)

Credit: The principles of human biochemical genetics / Harry Harris. Source: Wellcome Collection.

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    454 References SLY, w. s., QuiNTON, B. A., MCALLISTER, w. H. and RiMoiN, d. L. (1973). Isolated ß-g\u- curonidase deficiency: clinical report of a new mucopolysaccharidosis. J. Pediat. 82, 249. SMITH, D. H., CLEGG, J. В., WEATHERALL, D. J. and GILLES, H. M. (1973). Hereditary persist¬ ence of foetal haemoglobin associated with a yß fusion variant. Haemoglobin Kenya. Nature New Biol. 246, 184. smith, e. w. and torbert, j. v. (1958). Two abnormal haemoglobins with evidence for a new genetic locus for haemoglobin formation. Bull. Johns Hopkins Hosp. 102, 38. SMITH, J. M. (1968). 'Haldane's dilemma' and the rate of evolution. Nature (Lond.) 219, 1114. SMITH, J. M. (1970). Population size, polymorphism and the rate of non-Darwinian evolu¬ tion. Am. Naturalist 104, 231. smith, j. m. (1970). The causes of polymorphism. Symp.: Zool. Soc. Lond. No. 26, 371. smith, L. f. (1966). Species variation in the aminoacid sequence of insulin. Am. J. Med. 40, 662. SMITH, L. H., SULLIVAN, M. and HUGULEY, c. M. JR. (1961). Pyrimidine metabolism in man. IV. The enzymatic defect of oroticaciduria. J. Clin. Invest. 40, 656. SMITH, L. H., HUGL'LEY, c. M. JR. and BAIN, J. A. (1972). Hereditary orotic aciduria. !n: The Metabolic Basis of Inherited Disease, eds. J. B. Stanbury, J. B. Wyngaarden and D. S. Fredrickson. 3rd Edition. McGraw-Hill, New York. SMITH, M., HOPKiNSON, D. A. and HARRIS, H. (1971). Developmental changes and poly¬ morphisms in human alcohol dehydrogenase. Ann. Hum. Genet. Lond. 34, 251. smith, m., hopkinson, d. a. and harris, h. (1972). Alcohol dehydrogenase isozymes in adult human stomach and liver; evidence for activity of the ADHs locus. Ann. Hum. Genet. Lond. 35, 243. SMITH, M., HOPKINSON, D. A. and HARRIS, H. (1973). Studies on the subunit structure and molecular size of the human alcohol dehydrogenase isozymes determined by the different loci, ADHi, ADHi and ADHz. Ann. Hum. Genet. Lond. 36, 401. SMITH, s. E. and KYI, т. (1968). Inactivation of isoniazid in Burmese subjects. Nature (Lond.) 2/7, 1273. SMITHIES, o. (1955). Zone electrophoresis in starch gels: group variations in the serum proteins of normal human adults. Biochem. J. 61, 629. smithies, o. (1957). Variations in human serum /^-globulins. Nature (Lond.) 180, 1482. smithies, o. (1964). Chromosomal rearrangements and protein structure. Cold Spring Harbor Symp. Quant. Biol. 29, 309. smithies, o. (1967). Antibody variability. Science /57, 267. smithies, o. and connell, g. e. (1959). Biochemical aspects of the inherited variations in human serum haptoglobins and transferrins, in: Ciba Foundation Symposium on Biochemistry of Human Genetics, ed. G. E. Wolstenholme and С. M. O'Connor, Churchill, London. smithies, o., connell, g. e. and dixon, g. h. (1962a). Inheritance of haptoglobin subtypes. Am. J. Hum. Genet. 14, 14. smithies, o., connell, g. e. and dixon, g. h. (1962b). Chromosomal rearrangements and the evolution of haptoglobin genes. Nature (Lond.) 196, 232. smithies, o., connell, g. e. and dixon, g. h. (1966). Gene action in the human hapto¬ globins. I. Dissociation into constituent polypeptide chains. J. Mol. Biol. 21, 213.