Zobrazeno 1 - 10
of 19
pro vyhledávání: '"A Metaxatou-Mavromati"'
Autor:
Higgs, D. R., Pressley, L., Aldridge, B., Clegg, J. B., Weatherall, D. J., Cao, A., Hadjiminas, M. G., Kattamis, C., Metaxatou-Mavromati, A., Rachmilewitz, E. A., Sophocleous, T.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1981 Sep 01. 78(9), 5833-5837.
Externí odkaz:
https://www.jstor.org/stable/11563
Autor:
Amin, A. B., Pandya, N. L., Diwin, P. P., Darbre, P. D., Kattamis, C., Metaxatou-Mavromati, A., White, J. M., Wood, W. G., Clegg, J. B., Weatherall, D. J.
Publikováno v:
British Journal of Haematology; Dec1979, Vol. 43 Issue 4, p537-548, 12p
Autor:
Clegg, J. B., Metaxatou-Mavromati, A., Kattamis, C., Sofroniadou, K., Wood, W. G., Weatherall, D. J.
Publikováno v:
British Journal of Haematology; Dec1979, Vol. 43 Issue 4, p521-536, 16p
Autor:
Pressley, Lynne, Higgs, D.R., Aldridge, B., Metaxatou-Mavromati, A., Clegg, J.B., Weatheral1, D.J.
Publikováno v:
Nucleic Acids Research; 11/1/1980, Vol. 8 Issue 21, p4889-4898, 10p
Autor:
N. L. Pandya, John B. Clegg, P. P. Diwin, Christos Kattamis, J. M. White, A. B. Amin, D. J. Weatherall, Philippa D. Darbre, William G. Wood, A. Metaxatou-Mavromati
Publikováno v:
British Journal of Haematology. 43:537-548
One Arabic and two Indian patients with thalassaemia intermedia produce only Hb F for the G gamma type. Haemoglobin synthesis studies and genetic analysis indicate that they are homozygous for G gamma delta beta thalassaemia. The findings in these pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cad35a1c7a3acb6faf4170276eecf7d
https://doi.org/10.1111/j.1365-2141.1979.tb03786.x
https://doi.org/10.1111/j.1365-2141.1979.tb03786.x
Autor:
M G Hadjiminas, B. Aldridge, David J. Weatherall, Doug Higgs, J. B. Clegg, Antonio Cao, C Kattamis, L. Pressley, E A Rachmilewitz, A Metaxatou-Mavromati, T Sophocleous
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 78(9)
Restriction endonuclease mapping of nondeletion alpha-thalassemia determinants from a variety of racial groups showed no detectable abnormalities within a 40-kilobase region of the zeta-alpha globin gene cluster. By using a zeta-specific probe, we de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f17adca78c5c5b6a02c630b57b1b85c
https://pubmed.ncbi.nlm.nih.gov/6272319
https://pubmed.ncbi.nlm.nih.gov/6272319
Autor:
John B. Clegg, William G. Wood, A. Metaxatou-Mavromati, Christos Kattamis, David J. Weatherall, K. Sofroniadou
Publikováno v:
British journal of haematology. 43(4)
Haemoglobin F has been isolated from the red cells of individuals with the Greek form of hereditary persistence of fetal haemoglobin (HPFH), and the glycine/alanine composition of the gamma CB3 peptides determined. In contrast to previous reports we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::139f1ea697eaaba5ebe6002a7b836503
https://pubmed.ncbi.nlm.nih.gov/93488
https://pubmed.ncbi.nlm.nih.gov/93488
Autor:
A B, Amin, N L, Pandya, P P, Diwin, P D, Darbre, C, Kattamis, A, Metaxatou-Mavromati, J M, White, W G, Wood, J B, Clegg, D J, Weatherall
Publikováno v:
British journal of haematology. 43(4)
One Arabic and two Indian patients with thalassaemia intermedia produce only Hb F for the G gamma type. Haemoglobin synthesis studies and genetic analysis indicate that they are homozygous for G gamma delta beta thalassaemia. The findings in these pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cb341955b2f4927f406870fd99bf62d7
https://pubmed.ncbi.nlm.nih.gov/93489
https://pubmed.ncbi.nlm.nih.gov/93489
A new deletion causing alpha thalassemia has been characterised in a Greek family. Detailed mapping of the alpha gene complex shows that the deletion extends for 5.2 kb and removes the whole of the alpha 2 gene and the 5' end of the alpha 1 gene. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d62ffc4a3ef32bfe3e267330fb88854b
https://europepmc.org/articles/PMC324266/
https://europepmc.org/articles/PMC324266/
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