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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    440 References and genetic studies in cystinuria, observations on double heterozygotes of Genotype I/II. J. Clin. Invest. 50, 1961. MORRIS, M. D., FISHER, D. A. and FisER, R. (1966). Late onset branched chain ketoaciduria (maple syrup urine disease). Journal-Lancet 86, 149. MORRIS, M. D. and FISHER, D. A. (1967). Trypsinogen deficiency disease. Am. J. Diseases Children 114, 203. MORROW, G. (1967). Citrullinemia. Am. J. Diseases Children ÌI3, 157. MORROW, III. G., BARNES, L. A., CARDINALE, G. J., ABELES, R. H. and FLAKS, J. G. (1969). Congenital methylmalonic acidemia; enzymatic evidence för two forms of the disease. Proc. Natl. Acad. Sci. U.S. 63, 191. MORTON, N. E. (1964). Genetic studies of Northeastern Brazil. Cold Spring Harbor Symp. Quant. Biol. 29, 69. MOSER, H. w., EFRON, M. L., BROWN, H., DIAMOND, R. and NEUMANN, L. G. (1967). Arginino- succinicaciduria; Report of two new cases and demonstration of intermittent elevation of blood ammonia. Am. J. Med. 42, 9. MOTULSKY, A. G. (1964). Current concepts of the genetics of the thalassaemias. Cold Spring Harbor Symp. Quant. Biol. 29, 399. MOURANT, A, E. (1946). A 'new' human blood group antigen of frequent occurrence. Nature (Lond.) 158, 1У1. MOURANT, A. E., KOPEC, A. c. and DOMANiEwsKA-soBCZAK. (1971). Blood groups and blood clotting. Lancet /, 223. MOWBRAY, s., WATSON, B. and HARRIS, H. (1972). A search for electrophoretic variants of human adenine phosphoribosyl transferase. Ann. Hum. Genet. Lond. 36, 153. MUDD, s. H., iRREVERRE, F. and LASTER, L. (1967). Sulfite oxidase deficiency in man: dem¬ onstration of the enzymatic defect. Science 156, 1599. MUDD, s. H., FiNKELSTEiN, J. D. IRREVERRE, F. and LASTER, L. (1964). Homocystinuria: an enzymatic defect. Science 143, 1443. MUDD, S. H., EDWARDS, W. A., LOEB, P. M., BROWN, M. S. and LASTER, L. (1970). Homo- cystinuria due to cystathionine synthase deficiency: the effect of pyridoxine. J. Clin. Invest. 49, 1762. MUDD, S. H., UHLENDORF, B. W., FREEMAN, J. M., FINKELSTEIN, J. D. and SHIH, V. E. (1972). Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity. Biochem. Biophys. Res. Comm. 46, 905. MULLER, c. J. and KiNGMA, s. (1961). Haemoglobin Zurich Biochim. Biophys. Acta 50, 595. MURRAY, P., THOMSON, J. A., MCGIRR, E. M., WALLACE, T. J., MACDONALD, E. M. and MACCABAE, H. J. (1965). Absent and defective iodotyrosine deiodination. Lancet 1, 183. MYRiANTHOPOULOS, N. c. and ARONSON, s. M. (1966). Population dynamics of Tay-Sachs disease. L Reproductive fitness and selection. Am. J. Hum. Genet. 18, 313. MYRIANTHOPOULOS, N. c. and ARONSON, s. M. (1972). Population dynamics of Tay-Sachs disease. IL What confers the selective advantage upon the Jewish heterozygote? In: Sphingolipids, sphingolipidoses and allied disorders, eds.: B. W. Volk and S. M. Aronson. Plenum Press, New York. MYRIANTHOPOULOS, N. c., NAYLOR, A. F. and ARONSON, s. M. (1972). Founder effect in Tay- Sachs disease unlikely. Am. J. Hum. Genet. 24, 341. NABHOLZ, M., MiGGiANO, V. and BODMER, w. (1969). Genetic analysis with human-mouse