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