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Collins, F. S., Stoeckert, C. J., Serjeant, G. R., Forget, B. G., Weissman, S. M. (1984) G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene. Proceedings of the National Academy of Sciences, 81 (15) 4894-4898 doi:10.1073/pnas.81.15.4894

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Reference TypeJournal (article/letter/editorial)
TitleG gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene.
JournalProceedings of the National Academy of Sciences
AuthorsCollins, F. S.Author
Stoeckert, C. J.Author
Serjeant, G. R.Author
Forget, B. G.Author
Weissman, S. M.Author
Year1984 (August 1)Volume81
Issue15
PublisherProceedings of the National Academy of Sciences
DOIdoi:10.1073/pnas.81.15.4894Search in ResearchGate
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Mindat Ref. ID1436023Long-form Identifiermindat:1:5:1436023:1
GUID0
Full ReferenceCollins, F. S., Stoeckert, C. J., Serjeant, G. R., Forget, B. G., Weissman, S. M. (1984) G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene. Proceedings of the National Academy of Sciences, 81 (15) 4894-4898 doi:10.1073/pnas.81.15.4894
Plain TextCollins, F. S., Stoeckert, C. J., Serjeant, G. R., Forget, B. G., Weissman, S. M. (1984) G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene. Proceedings of the National Academy of Sciences, 81 (15) 4894-4898 doi:10.1073/pnas.81.15.4894
In(1984, August) Proceedings of the National Academy of Sciences Vol. 81 (15) Proceedings of the National Academy of Sciences

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Tuan, D., Feingold, E., Newman, M., Weissman, S. M., Forget, B. G. (1983) Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man. Proceedings of the National Academy of Sciences, 80 (22) 6937-6941 doi:10.1073/pnas.80.22.6937
FEINGOLD, ELISE A., COLLINS, FRANCIS S., METHERALL, JAMES E., STOECKERT, CHRISTIAN J., WEISSMAN, SHERMAN M., FORGET, BERNARD G. (1985) Molecular Analysis of Deletion and Nondeletion Hereditary Persistence of Fetal Hemoglobin and Identification of a New Mutation Causing ?-Thalassemia. Annals of the New York Academy of Sciences, 445 (1) 159-169 doi:10.1111/j.1749-6632.1985.tb17185.x
Antonarakis, S. E., Boehm, C. D., Serjeant, G. R., Theisen, C. E., Dover, G. J., Kazazian, H. H. (1984) Origin of the beta S-globin gene in blacks: the contribution of recurrent mutation or gene conversion or both. Proceedings of the National Academy of Sciences, 81 (3) 853-856 doi:10.1073/pnas.81.3.853
Collins, Francis S., Metherall, James E., Yamakawa, Minoru, Pan, Julian, Weissman, Sherman M., Forget, Bernard G. (1985) A point mutation in the Aγ-globin gene promoter in Greek hereditary persistence of fetal haemoglobin. Nature, 313 (6000). 325-326 doi:10.1038/313325a0
Charache, S., Dover, G., Smith, K., Talbot, C. C., Moyer, M., Boyer, S. (1983) Treatment of sickle cell anemia with 5-azacytidine results in increased fetal hemoglobin production and is associated with nonrandom hypomethylation of DNA around the gamma-delta-beta-globin gene complex. Proceedings of the National Academy of Sciences, 80 (15) 4842-4846 doi:10.1073/pnas.80.15.4842
Barry, G. F., Rogers, S. G., Fraley, R. T., Brand, L. (1984) Identification of a cloned cytokinin biosynthetic gene. Proceedings of the National Academy of Sciences, 81 (15) 4776-4780 doi:10.1073/pnas.81.15.4776
Kafatos, F. C., Efstratiadis, A., Forget, B. G., Weissman, S. M. (1977) Molecular evolution of human and rabbit beta-globin mRNAs. Proceedings of the National Academy of Sciences, 74 (12) 5618-5622 doi:10.1073/pnas.74.12.5618
TANAKA, MINORU, NOLAN, JUDITH A., BHARGAVA, AJAY K., ROOD, KIRSTEN, COLLINS, FRANCIS S., WEISSMAN, SHERMAN M., FORGET, BERNARD G., CHAMBERLAIN, JOHN W. (1990) Expression of Human Globin Genes in Transgenic Mice Carrying the ?-Globin Gene Cluster with a Mutation CausingG??+Hereditary Persistence of Fetal Hemoglobin. Annals of the New York Academy of Sciences, 612 (1) 167-178 doi:10.1111/j.1749-6632.1990.tb24303.x
Bernards, R., Little, P. F., Annison, G., Williamson, R., Flavell, R. A. (1979) Structure of the human G gamma-A gamma-delta-beta-globin gene locus. Proceedings of the National Academy of Sciences, 76 (10) 4827-4831 doi:10.1073/pnas.76.10.4827
Ottolenghi, S., Giglioni, B., Taramelli, R., Comi, P., Mazza, U., Saglio, G., Camaschella, C., Izzo, P., Cao, A., Galanello, R., Gimferrer, E., Baiget, M., Gianni, A. M. (1982) Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?. Proceedings of the National Academy of Sciences, 79 (7) 2347-2351 doi:10.1073/pnas.79.7.2347
Driscoll, M. C., Dobkin, C. S., Alter, B. P. (1989) Gamma delta beta-thalassemia due to a de novo mutation deleting the 5' beta-globin gene activation-region hypersensitive sites. Proceedings of the National Academy of Sciences, 86 (19) 7470-7474 doi:10.1073/pnas.86.19.7470
 
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