BEŞBAŞ, N. Et Al. 2009. A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis. EUROPEAN JOURNAL OF PEDIATRICS , vol.168, no.12 , 1449-1454.

BEŞBAŞ, N., Draaken, M., Ludwig, M., DEREN, Ö., ORHAN, D., BİLGİNER, Y., ... ÖZALTIN, F.(2009). A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis. EUROPEAN JOURNAL OF PEDIATRICS , vol.168, no.12, 1449-1454.

BEŞBAŞ, NESRİN Et Al. "A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis," EUROPEAN JOURNAL OF PEDIATRICS , vol.168, no.12, 1449-1454, 2009

BEŞBAŞ, NESRİN Et Al. "A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis." EUROPEAN JOURNAL OF PEDIATRICS , vol.168, no.12, pp.1449-1454, 2009

BEŞBAŞ, N. Et Al. (2009) . "A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis." EUROPEAN JOURNAL OF PEDIATRICS , vol.168, no.12, pp.1449-1454.

@article{article, author={NESRİN BEŞBAŞ Et Al. }, title={A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis}, journal={EUROPEAN JOURNAL OF PEDIATRICS}, year=2009, pages={1449-1454} }