M. Boussiou

发表

Carrier Screening and Prenatal Diagnosis of Hemoglobinopathies. A Study of Indigenous and Immigrant Couples in Northern Greece, Over the Last 5 Years

E. Voskaridou, E. Plata, K. Sinopoulou, 2008, Hemoglobin.

Evaluation of the BeTha Gene 1 Kit for the Qualitative Detection of the Eight Most Common Mediterranean β‐Thalassemia Mutations

R. Galanello, A. Maggio, L. Ugozzoli, 1998, American journal of hematology.

Beta-thalassaemia mutations and the underlying beta gene cluster haplotypes in the Greek population.

M. Papadakis, D. Loukopoulos, P. Kollia, 1992, Gene geography : a computerized bulletin on human gene frequencies.

The origin of the sickle mutation in Greece; evidence from beta S globin gene cluster polymorphisms.

D. Loukopoulos, P. Fessas, M. Boussiou, 1991, Hemoglobin.

The molecular heterogeneity of β-thalassemia in Greece

E. Plata, K. Sinopoulou, P. Tsaftaridis, 2008 .

Structural study of hemoglobin Knossos, beta 27 (B9) Ala leads to Ser. A new abnormal hemoglobin present as a silent beta-thalassemia.

D. Loukopoulos, Y. Blouquit, F. Galactéros, 1982, FEBS letters.

PRENATAL DIAGNOSIS OF X‐LINKED SPINAL AND BULBAR MUSCULAR ATROPHY IN A GREEK FAMILY

C. Yapijakis, D. Vassilopoulos, E. Kapaki, 1996, Prenatal diagnosis.

Prenatal Diagnosis of Thalassemia and Hb S Syndromes in Greece: An Evaluation of 1500 Cases a

D. Loukopoulos, J. Panourgias, P. Fessas, 1985, Annals of the New York Academy of Sciences.

Prenatal Diagnosis of Thalassemia and of the Sickle Cell Syndromes in Greece a

M. Papadakis, D. Loukopoulos, P. Kollia, 1990, Annals of the New York Academy of Sciences.

Structural study of hemoglobin Knossos, p27 (B9) Ala-+Ser A new abnormal hemoglobin present as a silent /3-thalassemia N. Arous, F. Galacteros, Ph. Fessas+, D. Loukopoulos+, Y. Blouquit, G. Komis+, M. Sellaye,

J. Rosa, M. Boussiou, 1982 .

Gγ-196 C→T, Aγ-201 C→T: Two novel mutations in the promoter region of the γ-globin genes associated with nondeletional hereditary persistence of fetal hemoglobin in Greece

K. Sinopoulou, P. Karababa, M. Boussiou, 2008 .

G gamma-196 C-->T, A gamma-201 C-->T: two novel mutations in the promoter region of the gamma-globin genes associated with nondeletional hereditary persistence of fetal hemoglobin in Greece.

K. Sinopoulou, P. Karababa, M. Boussiou, 2008, Blood cells, molecules & diseases.

An improved method for the diagnostic approach of α+‐thalassaemia

H. Papadaki, G. Eliopoulos, P. Karababa, 2007, International journal of laboratory hematology.

Selective survival of only the healthy fetus following prenatal diagnosis of thalassaemia major in binovular twin gestation

D. Loukopoulos, J. Panourgias, A. Antsaklis, 1984, Prenatal Diagnosis.