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pro vyhledávání: '"Ch Skentou"'
Autor:
S. Amenta, Ch Skentou, A. Ntouflia, Thomas Liehr, N. Chaliasos, Emmanouil Manolakos, Eleftherios Anastasakis, Helena Fryssira, Ioannis Papoulidis, Stavroula Psoni, Eirini Tsoutsou
Publikováno v:
Molecular Cytogenetics
Background FOXG1 gene mutations have been associated with the congenital variant of Rett syndrome (RTT) since the initial description of two patients in 2008. The on-going accumulation of clinical data suggests that the FOXG1-variant of RTT forms a d
Autor:
Fryssira H; Medical genetics, School of Medicine, National and Kapodistrian University of Athens, 'Aghia Sophia' Children's Hospital, Athens, Greece., Tsoutsou E; Medical genetics, School of Medicine, National and Kapodistrian University of Athens, 'Aghia Sophia' Children's Hospital, Athens, Greece., Psoni S; Medical genetics, School of Medicine, National and Kapodistrian University of Athens, 'Aghia Sophia' Children's Hospital, Athens, Greece., Amenta S; 'Mitera' Maternity Hospital, Athens, Greece., Liehr T; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Jena, Germany., Anastasakis E; Hellenic Navy Hospital, Deinokratous 70, Athens, 11521 Greece., Skentou Ch; 'Mitera kai emvrio' Medical centre, Larisa, Greece., Ntouflia A; 'Access to Genome' Clinical Laboratory Genetics, Athens Thessaloniki, Greece., Papoulidis I; 'Access to Genome' Clinical Laboratory Genetics, Athens Thessaloniki, Greece., Manolakos E; 'Access to Genome' Clinical Laboratory Genetics, Athens Thessaloniki, Greece ; Department of Medical Genetics, Binaghi Hospital, University of Cagliari, Cagliari, Italy., Chaliasos N; Child Health Department, University Hospital of Ioannina (UHI), Ioannina, Greece.
Publikováno v:
Molecular cytogenetics [Mol Cytogenet] 2016 Aug 02; Vol. 9, pp. 55. Date of Electronic Publication: 2016 Aug 02 (Print Publication: 2016).