C. Karadimas

FGFR3 related skeletal dysplasias diagnosed prenatally by ultrasonography and molecular analysis: Presentation of 17 cases

A. Konstantinidou, S. Sifakis, V. Velissariou, 2011, American journal of medical genetics. Part A.

Central nervous system involvement in four patients with Charcot-Marie-Tooth disease with connexin 32 extracellular mutations

D. Avramopoulos, M. Panas, D. Vassilopoulos, 1998, Journal of neurology, neurosurgery, and psychiatry.

Hereditary neuropathy with liability to pressure palsies: the same molecular defect can result in diverse clinical presentation

C. Yapijakis, V. Zis, G. Paraskevas, 1996, Journal of Neurology.

FGFR3 related skeletal dysplasias diagnosed prenatally by ultrasonography and molecular analysis: Presentation of 17 cases

A. Konstantinidou, S. Sifakis, V. Velissariou, 2011, American journal of medical genetics. Part A.