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Helen Frysira
Helen Frysira
National and Kapodistrian University of Athens
Genetics
Intellectual disability
Gene
Biology
Medicine
4
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44
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Development of a multidisciplinary clinic of neurofibromatosis type 1 and other neurocutaneous disorders in Greece. A 3-year experience
2019
Postgraduate Medicine
Eleftheria Kokkinou
Kleoniki Roka
Alexis Alexopoulos
Efthymia Tsina
Ioannis Nikas
Panagiotis Ν. Krallis
Ioanna Thanopoulou
Lambrini Nasi
Evanthia A. Makrygianni
Eirini Tsoutsou
Konstantina Kosma
Maria Tsipi
Maria Tzetis
Helen Frysira
Antonis Kattamis
Roser Pons
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Citations (3)
Microdeletion and microduplication 17q21.31 plus an additional CNV, in patients with intellectual disability, identified by array-CGH.
2012
Gene
Sophia Kitsiou-Tzeli
Helen Frysira
Krinio Giannikou
Areti Syrmou
Konstantina Kosma
Georgia Kakourou
Eleni Leze
Christalena Sofocleous
Emmanuel Kanavakis
Maria Tzetis
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Citations (26)
The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization
2012
Expert Review of Molecular Diagnostics
Maria Tzetis
Sofia Kitsiou-Tzeli
Helen Frysira
Athena Xaidara
Emmanuel Kanavakis
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Citations (15)
Molecular investigation of Angelman syndrome in Greece. Screening for UBE3A mutations: preliminary results
2008
Annals of General Psychiatry
Evmorfia Tzagaraki
Christalena Sofocleous
Nikolaos Vogiatzakis
Sofia Kitsiou
Helen Frysira
George N. Goulielmos
Emmanouil Kanavakis
Ariadni Mavrou
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