Genetic basis of the thalassaemia diseases.
作者： V. M. INGRAM , A. O. W. STRETTON
DOI: 10.1038/1841903A0
关键词:
摘要:
nature.com
cabdirect.org
harvard.edu
sci-hub.se 参考文章(27)
J. A. HUNT, Identity of the α-Chains of Adult and Fœtal Human Hæmoglobins Nature. ,vol. 183, pp. 1373- 1375 ,(1959) , 10.1038/1831373A0
W. W. Zuelzer, E. Kaplan, Erythrocyte survival studies in childhood. II. Studies in Mediterranean anemia. Journal of Laboratory and Clinical Medicine. ,vol. 36, pp. 517- ,(1950)
Harvey A. Itano, The Human Hemoglobins: Their Properties and Genetic Control Advances in Protein Chemistry. ,vol. 12, pp. 215- 268 ,(1957) , 10.1016/S0065-3233(08)60117-5
H. C. SCHWARTZ, T. H. SPAET, W. W. ZUELZER, J. V. NEEL, A. R. ROBINSON, S. F. KAUFMAN, Combinations of hemoglobin G, hemoglobin S and thalassemia occurring in one family. Blood. ,vol. 12, pp. 238- 250 ,(1957) , 10.1182/BLOOD.V12.3.238.238
E. SILVESTRONI, I. BIANCO, Genetic aspects of sickle cell anemia and microdrepanocytic disease. Blood. ,vol. 7, pp. 429- 435 ,(1952) , 10.1182/BLOOD.V7.4.429.429
ARNO G. MOTULSKY, Genetic and haematological significance of haemoglobin H. Nature. ,vol. 178, pp. 1055- 1056 ,(1956) , 10.1038/1781055B0
Herbert S. Rhinesmith, W. A. Schroeder, Linus Pauling, A Quantitative Study of the Hydrolysis of Human Dinitrophenyl(DNP)globin: The Number and Kind of Polypeptide Chains in Normal Adult Human Hemoglobin Journal of the American Chemical Society. ,vol. 79, pp. 4682- 4686 ,(1957) , 10.1021/JA01574A028
H. G. KUNKEL, G. WALLENIUS, New hemoglobin in normal adult blood. Science. ,vol. 122, pp. 288- 288 ,(1955) , 10.1126/SCIENCE.122.3163.288
H. A. Itano, S. J. Singer, ON DISSOCIATION AND RECOMBINATION OF HUMAN ADULT HEMOGLOBINS A, S, AND C Proceedings of the National Academy of Sciences. ,vol. 44, pp. 522- 529 ,(1958) , 10.1073/PNAS.44.6.522
A. Rich, Studies on the Hemoglobin of Cooley's Anemia and Cooley's Trait. Proceedings of the National Academy of Sciences of the United States of America. ,vol. 38, pp. 187- 196 ,(1952) , 10.1073/PNAS.38.3.187