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Published in BMC medical genomics (25.03.2024)
Published in BMC medical genomics (25.03.2024)
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Inherited metabolic disorders in Cyprus
Georgiou, Theodoros, Petrou, Petros P., Malekkou, Anna, Ioannou, Ioannis, Gavatha, Marina, Skordis, Nicos, Nicolaidou, Paola, Savvidou, Irini, Athanasiou, Emilia, Ourani, Sofia, Papamichael, Elena, Vogazianos, Marios, Dionysiou, Maria, Mavrikiou, Gabriella, Grafakou, Olga, Tanteles, George A., Anastasiadou, Violetta, Drousiotou, Anthi
Published in Molecular genetics and metabolism reports (01.06.2024)
Published in Molecular genetics and metabolism reports (01.06.2024)
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Minimally symptomatic mcardle disease, expanding the genotype-phenotype spectrum
Petrou, Petros, Pantzaris, Marios, Dionysiou, Maria, Drousiotou, Anthi, Kyriakides, Theodoros
Published in Muscle & nerve (01.11.2015)
Published in Muscle & nerve (01.11.2015)
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Molecular analysis of Cypriot patients with Glutaric aciduria type I: Identification of two novel mutations
Georgiou, Theodoros, Nicolaidou, Paola, Hadjichristou, Anastasia, Ioannou, Rodothea, Dionysiou, Maria, Siama, Elli, Chappa, Georgia, Anastasiadou, Violetta, Drousiotou, Anthi
Published in Clinical biochemistry (01.09.2014)
Published in Clinical biochemistry (01.09.2014)
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The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening
Georgiou, Theodoros, Ho, Gladys, Vogazianos, Marios, Dionysiou, Maria, Nicolaou, Alexia, Chappa, Georgia, Nicolaides, Paola, Stylianidou, Goula, Christodoulou, John, Drousiotou, Anthi
Published in Clinical biochemistry (01.05.2012)
Published in Clinical biochemistry (01.05.2012)
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