Nal, N. Et Al. 2003. A rare mutation (codon 22 A>C) in beta-thalassemia and its prenatal diagnosis. European Human Genetics Conference 2003 , (Birmingham, United Kingdom), 241.

Nal, N., Sargin, F., MANGUOĞLU , E., KESER, İ., Yesilipek, A., MENDİLCİOĞLU, İ. İ., ... Yesilipek, A.(2003). A rare mutation (codon 22 A>C) in beta-thalassemia and its prenatal diagnosis . European Human Genetics Conference 2003 (pp.241). Birmingham, United Kingdom

Nal, N Et Al. "A rare mutation (codon 22 A>C) in beta-thalassemia and its prenatal diagnosis," European Human Genetics Conference 2003, Birmingham, United Kingdom, 2003

Nal, N Et Al. "A rare mutation (codon 22 A>C) in beta-thalassemia and its prenatal diagnosis." European Human Genetics Conference 2003 , Birmingham, United Kingdom, pp.241, 2003

Nal, N. Et Al. (2003) . "A rare mutation (codon 22 A>C) in beta-thalassemia and its prenatal diagnosis." European Human Genetics Conference 2003 , Birmingham, United Kingdom, p.241.

@conferencepaper{conferencepaper, author={N Nal Et Al. }, title={A rare mutation (codon 22 A>C) in beta-thalassemia and its prenatal diagnosis}, congress name={European Human Genetics Conference 2003}, city={Birmingham}, country={United Kingdom}, year={2003}, pages={241} }