Recurrent increased nuchal translucency: a first trimester presentation of familial 13p satellite deletion
I Uzun, R Has, E Alici, M Ozdemir, C Inan, S Erzincan
Difficulties in Diagnosing Fabry Disease in Patients with Unexplained Left Ventricular Hypertrophy (LVH): Is the Novel GLA Gene Mutation a Pathogenic Mutation or Polymorphism?
N Aladağ, H Ali Barman, A Şipal, T Akbulut, M Özdemir, S Ceylaner