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Sfoglia per Autore "Kontodiou, M."

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    • Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature 

      Sifakis, S.; Manolakos, E.; Vetro, A.; Kappou, D.; Peitsidis, P.; Kontodiou, M.; Garas, A.; Vrachnis, N.; Konstandinidou, A.; Zuffardi, O.; Orru, S.; Papoulidis, I. (2012)
      Wolf-Hirschhorn syndrome (WHS) is a well known genetic condition caused by a partial deletion of the short arm of chromosome 4. The great variability in the extent of the 4p deletion and the possible contribution of ...

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      Kitsiou-Tzeli, S.; Manolakos, E.; Lagou, M.; Kontodiou, M.; Kosyakova, N.; Ewers, E.; Weise, A.; Garas, A.; Orru, S.; Liehr, T.; Metaxotou, A. (2009)
      Background: The heterogeneous group of small supernumerary marker chromosomes (sSMCs) presents serious counseling problems, especially if they are present de novo and diagnosed prenatally. The incidence has been estimated ...