Search Results - "Tadmouri, G.O."

Comorbidity in the Tunisian population by Romdhane, L., Messaoud, O., Bouyacoub, Y., Kerkeni, E., Naouali, C., Cherif Ben Abdallah, L., Tiar, A., Charfeddine, C., Monastiri, K., Chabchoub, I., Hachicha, M., Tadmouri, G.O., Romeo, G., Abdelhak, S.

“…Genetic diseases in the Tunisian population represent a real problem of public health as their spectrum encompasses more than 400 disorders. Their frequency…”
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Molecular and population genetic analyses of β‐Thalassemia in Turkey by Tadmouri, G.O., Tüzmen, Ş., Özçelik, H., Özer, A., Baig, S.M., Senga, E.B., Başak, A.N.

“…In this report we describe the molecular analysis of 795 chromosomes derived from unrelated Turkish β‐thalassemia and sickle cell anemia carriers identified in…”
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A rare mutation [IVS-I-130 (G-A)] in a Turkish ?-thalassemia major patient by Tadmouri, G.O., Bileno?lu, O., Kantarc?, S., Kayserili, H., Perrin, P., Ba?ak, A.N.

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A rare mutation lIVS-l-130(G-A)l in a Turkish beta-thalassemia major patient by G.O., Tadmouri, Bilenoglu, O., Kantarci, S., Kayserili, H., Perrin, P., Basak, A.N.

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A rare mutation [IVS‐I‐130 (G‐A)] in a Turkish β‐thalassemia major patient by Tadmouri, G.O., Bilenoğlu, O., Kantarcı, S., Kayserili, H., Perrin, P., Başak, A.N.

“…Here we describe the identification of the rare β‐thalassemia mutation IVS‐I‐130 (G‐A) for the first time in Turkey. The hematological evaluation of the…”
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