Folyóiratcikkek tallózása szerző szerint "Olbrich H"

A találatok rendezése: Rendezés: Találatok:

  • Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients 
    Horvath J; Fliegauf M; Olbrich H; Kispert A; King SM; Mitchison H; Zariwala MA; Knowles MR; Sudbrak R; Fekete, György; Neesen J; Reinhardt R; Omran H (2005)
    Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder characterized by chronic infections of the upper and lower airways, randomization of left/right body asymmetry, and reduced fertility. The phenotype ...
  • Recessive HYDIN Mutations Cause Primary Ciliary Dyskinesia without Randomization of Left-Right Body Asymmetry 
    Olbrich H; Schmidts M; Werner C; Onoufriadis A; Loges NT; Bánki, Nóra Fanni; Shoemark, A; Burgoyne, T; Turki, S A; Hurles, M E; UK10K Consortium; Köhler, G; Schroeder, J; Nürnberg, G; Nürnberg, P; Chung, E M; Reinhardt, R; Marthin, J K; Nielsen, K G; Mitchison, M H; Omran, H (2012)
    Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder characterized by defective cilia and flagella motility. Chronic destructive-airway disease is caused by abnormal respiratory-tract ...