ARTAN, S. Et Al. 2014. A rare case with De Novo Isochromosome 18p Syndrome. European Human Genetics Conference 2014 , (Milan, Italy), 448.

ARTAN, S., ERZURUMLUOĞLU, E., ÇARMAN, K. B., GÜMÜŞ, E., ÖZDEMİR, M., DURAK ARAS, B., ... aynacı, s.(2014). A rare case with De Novo Isochromosome 18p Syndrome . European Human Genetics Conference 2014 (pp.448). Milan, Italy

ARTAN, SEVİLHAN Et Al. "A rare case with De Novo Isochromosome 18p Syndrome," European Human Genetics Conference 2014, Milan, Italy, 2014

ARTAN, SEVİLHAN Et Al. "A rare case with De Novo Isochromosome 18p Syndrome." European Human Genetics Conference 2014 , Milan, Italy, pp.448, 2014

ARTAN, S. Et Al. (2014) . "A rare case with De Novo Isochromosome 18p Syndrome." European Human Genetics Conference 2014 , Milan, Italy, p.448.

@conferencepaper{conferencepaper, author={SEVİLHAN ARTAN Et Al. }, title={A rare case with De Novo Isochromosome 18p Syndrome}, congress name={European Human Genetics Conference 2014}, city={Milan}, country={Italy}, year={2014}, pages={448} }