A Novel NKX3 2 Mutation Associated With Spondylo Megaepiphyseal Metaphyseal Dysplasia In A Neonate A Rare Clinical Entity


ŞİMŞEK KİPER P. Ö. , YAVUZ Ş., ÜTİNE G. E. , SOYER T. , KORKMAZ TOYGAR A., ALİKAŞİFOĞLU M. , ...More

International Skeletal Dysplasia Society 12th Biennial Meeting, 29 July - 01 August 2015

  • Publication Type: Conference Paper / Full Text