Zobrazeno 1 - 10
of 19
pro vyhledávání: '"J. F. Codrington"'
Autor:
Ph. Beris, Adekunle Adekile, J. F. Codrington, Louis D. Wadsworth, H-W. Li, Gino Schilirò, Titus H.J. Huisman
Publikováno v:
Hemoglobin. 15:77-84
A method of identifying delta chain variants using relatively small volumes of blood is described. The procedure consists of the amplification of two segments of genomic DNA with two sets of delta chain specific primers and sequencing of the three ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d00650c5027c9db9224bba591a6291e8
https://doi.org/10.3109/03630269109072486
https://doi.org/10.3109/03630269109072486
Publikováno v:
Blood. 76:1246-1249
Hb A2 and its variant B2 (alpha 2 delta 2(16)(A13)Gly----Arg) were quantitated in the blood of subjects with three different types of beta- thalassemia and with the delta-B2 anomaly in cis or in trans to the beta-thalassemia determinant. In one famil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcf17fdd021ccaf43d6bda61e9520f0c
https://doi.org/10.1182/blood.v76.6.1246.bloodjournal7661246
https://doi.org/10.1182/blood.v76.6.1246.bloodjournal7661246
Autor:
I Rodriguez, Ferdane Kutlar, Brooke B. Webber, J. B. Wilson, JT Prchal, J. F. Codrington, J. M. De Pablos, Abdullah Kutlar, H. Hu, KM Hall
Publikováno v:
Blood. 75:1883-1887
Two unstable hemoglobins (Hbs) causing rather severe hemolytic anemia have been characterized. The beta chain of Hb Birmingham, found in an adult black man, is characterized by the loss of -Leu-Ala-His-Lys- at positions 141, 142, 143, and 144 and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::863c73306e999cc7a536fc8b0f70b3f2
https://doi.org/10.1182/blood.v75.9.1883.bloodjournal7591883
https://doi.org/10.1182/blood.v75.9.1883.bloodjournal7591883
Autor:
J. H. Wisse, J. F. Codrington, Ferdane Kutlar, J. Anijs, Titus H.J. Huisman, H.-W. Li, F. A. Codrington, M. Ramachandran
Publikováno v:
Acta Haematologica. 84:135-138
Hematological and hemoglobin composition data are presented for 14 members of a Surinam family (and for 1 unrelated subject) with either a β-thalassemia heterozygosity [5 with the -29 (A – G) β+
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6a77d849e60145b146ec423ed275374
https://doi.org/10.1159/000205050
https://doi.org/10.1159/000205050
Publikováno v:
Hemoglobin. 14:491-497
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cb3cb471da00aaf6ffe5987fcba928e
https://doi.org/10.3109/03630269009005802
https://doi.org/10.3109/03630269009005802
Autor:
Ferdane Kutlar, D. R. Harkness, Abdullah Kutlar, J. F. Codrington, M. Harkness, J. B. Wilson, Brooke B. Webber, Titus H.J. Huisman
Publikováno v:
Hemoglobin. 14:479-489
A severe hemolytic anemia with microcytosis and hypochromia was present in a young adopted Indian patient. Reversed phase high performance liquid chromatographic methodology and heat stability tests detected an unstable α chain which was present in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2514346611332229a898c849192b9438
https://doi.org/10.3109/03630269009005801
https://doi.org/10.3109/03630269009005801
Autor:
C, Oner, A J, Dimovski, N F, Olivieri, G, Schiliro, J F, Codrington, S, Fattoum, A D, Adekile, R, Oner, G T, Yüregir, C, Altay
Publikováno v:
Human genetics. 89(1)
We have determined the beta S haplotypes in 709 patients with sickle cell anemia, 30 with SC disease, 91 with S-beta-thalassemia, and in 322 Hb S heterozygotes from different countries. The methodology concerned the detection of mutations in the prom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6eabf82a7fd35c837d5ff63eb2a5e4d4
https://pubmed.ncbi.nlm.nih.gov/1577473
https://pubmed.ncbi.nlm.nih.gov/1577473
Publikováno v:
Blood. 76(6)
Hb A2 and its variant B2 (alpha 2 delta 2(16)(A13)Gly----Arg) were quantitated in the blood of subjects with three different types of beta-thalassemia and with the delta-B2 anomaly in cis or in trans to the beta-thalassemia determinant. In one family
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::54ed7e8cf1a6c6b96d91c1d5b942383f
https://pubmed.ncbi.nlm.nih.gov/1698102
https://pubmed.ncbi.nlm.nih.gov/1698102
Autor:
J. M. Gonzalez-Redondo, O. Josifovska, Titus H.J. Huisman, N. Nikolov, J. F. Codrington, Georgi D. Efremov, C. Oner
Publikováno v:
British journal of haematology. 75(2)
Hb Icaria-Hb H disease was observed in a Yugoslavian teenager who exhibited moderate anaemia with severe microcytosis and hypochromia and 16% Hb H. Four of his relatives were Hb Icaria heterozygotes; their haematological data were comparable to those
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f8e58dbbc2919b3ccb3facf066da8cf
https://pubmed.ncbi.nlm.nih.gov/2372512
https://pubmed.ncbi.nlm.nih.gov/2372512
Publikováno v:
Hemoglobin. 14(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::623652eea50655a4a54ee1798546cc9b
https://pubmed.ncbi.nlm.nih.gov/2079430
https://pubmed.ncbi.nlm.nih.gov/2079430