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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    References 447 QUICK, С. В., FISHER, R. A. and HARRIS, H. (1974). A kinetic study of the isozymes determined by the three phosphoglucomutase loci, PGMi, PCЛ/г and PGM3. Europ. J. of Biochem. 42, 511. RACE, c., ziDERMAN, D. and WATKiNS, w. M. (1968). An a-D-galactosyltransferase associated with the blood group В character. Biochem. J. /07, 733. RACE, R. R. (1971). is the Xg blood group locus subject to inactivation? Proc. Fourth International Congress of Human Genetics, p. 311, Excerpta Medica, Amsterdam. RACE, R. R. and SANGER, R. (1968). Blood groups in man. 5th edition. Blackwell, Oxford. RAMOT, в., BEN-BASSAT, I. and SHCHORY, J. (1969). New glucose-6-phosphate dehydrogenase variants observed in Israel and their association with congenital non-spherocytic haemolytic anaemia. J. Lab. Clin. Med. 74, 895. RAMOT, B. and BRÖK, F. (1964). A new glucose-6-phosphate dehydrogenase mutant (Tel- Hashomer mutant). Ann. Hum. Genet. Lond. 28, 167. RAMOT, в., FISHER, S., SZEINBERG, A., ADAM, A., SHEBA, C. and GAFNI, D. (1959). A Study of subjects with glucose-6-phosphate dehydrogenase deficiency. 11. Investigation of leucocyte enzymes. J. Clin. Invest. 38, 2234. RANNEY, H. M., JACOBS, A. s., UDEM, L. and ZALUSKY, R. (1968). Hemoglobin Riverdale- Bronx, an unstable hemoglobin resulting from the substitution of arginine for glycine at helical residue B6 of the ß polypeptide chain. Biochim. Biophys. Res. Comm. 33, 1004. RANNEY, H. M., JACOBS, A. s., BRADLEY, T. B. and CORDOVA, F. A. (1963). A 'new' Variant of haemoglobin Аг and its segregation in a family with haemoglobin S. Nature (Lond.) 197, 614. RAPER, A. B. (1956). Sickling in relation to morbidity from malaria and other diseases. Brit. Med. J. /, 965. RAPER, A. В., GAMMACK, D. В., HUEHNS, E. R. and SHOOTER, E. M. (1960). Four haemoglobins in one individual. A study of the genetic interaction of Hb G and Hb С. Brit. Med. J. 2, 1257. RAPLEY, s., ROBSON, E. В. and HARRIS, H. (1967). Data on the incidence, segregation and linkage relations of the adenylate kinase (AK) polymorphism. Ann. Hum. Genet. Lond. 31, 237. RASMUSSEN, K. (1968). Phosphorylethanolamine and hypophosphatasia. Danish Med. Bull. 75 (supplement). RATHBUN, J. c. (1948). Hypophosphatasia, a new development anomaly. Amer. J. Diseases Children 75, 822. RATHBUN, J. C., MACDONALD, J. W., ROBINSON, H. M. and WANKLIN, J. M. (1961). HypophoS- phatasia: a genetic study. Arch. Disease Childhood 36, 540. RATTAZZi, M. c., MARKS, J. s. and DAVIDSON, R. G. (1973). Electrophoresis of arylsulfatase from normal individuals and patients with metachromatic leukodystrophy. Am. J. Hum. Genet. 25, 310. REED, C. S., HAMPSON, R., GORDON, S., JONES, R. T., NOVY, M. J., BRIMHALL, В., EDWARDS, M. J. and KOLER, R. D. (1968). Erythrocytosis secondary to increased oxygen affinity of a mutant hemoglobin, hemoglobin Kempsey. Blood 31, 623. REED, T. E. (1968). Research on blood groups and selection from the Child Health and Development Studies, Oakland, California. III. Couple mating type and reproductive performance. Am. J. Hum. Genet. 20, 129.