Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Afrodite Loutradi-Anagnostou"'
Publikováno v:
Human Mutation. 9:465-472
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fc6ae89dc05ddd66ea741b19b426a85
https://doi.org/10.1002/(sici)1098-1004(1997)9:5<465::aid-humu14>3.3.co
https://doi.org/10.1002/(sici)1098-1004(1997)9:5<465::aid-humu14>3.3.co
Publikováno v:
Human Mutation. 9:465-472
A scanning strategy for the detection of δ-globin gene mutations and polymorphisms is presented. This procedure is based on the denaturing gradient gel electrophoresis (DGGE) of four different artificially amplified DNA fragments which cover the pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54fafbfa52da8edb19fab51f4b53d81e
https://doi.org/10.1002/(sici)1098-1004(1997)9:5<465::aid-humu14>3.0.co
https://doi.org/10.1002/(sici)1098-1004(1997)9:5<465::aid-humu14>3.0.co
Autor:
Elisavet Papapanagiotou, Olga Drakoulakou, Manoussos N. Papadakis, Afrodite Loutradi-Anagnostou
Publikováno v:
Human Mutation. 9:344-347
δ-Thalassemia reduces the expected HbA2 percentage, altering the normal as well as the β-thalassemia trait phenotype. An attempt to elucidate the molecular basis of δ-thalassemia in the Greek population, revealed two cases with unknown molecular d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5af3c9dacc7ba69d4448607c14cb3ed3
https://doi.org/10.1002/(sici)1098-1004(1997)9:4<344::aid-humu7>3.0.co
https://doi.org/10.1002/(sici)1098-1004(1997)9:4<344::aid-humu7>3.0.co