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Diabetic Medicine : a Journal of the British Diabetic Association|March 31, 2004
Severe hypertriglyceridaemia in diabetic ketoacidosis: clinical and genetic studyC Karagianni, S Stabouli, K Roumeliotou, et al.
Prenatal Diagnosis|November 8, 2007
Noninvasive prenatal diagnosis of beta-thalassaemia using individual fetal erythroblasts isolated from maternal blood after enrichmentA Kolialexi, C Vrettou, J Traeger-Synodinos, et al.
Prenatal Diagnosis|February 9, 2007
Two-way trafficking of Annexin V positive cells between mother and fetus: determination of apoptosis at deliveryA Kolialexi, G Th Tsangaris, A Anagnostopoulos, et al.
British Journal of Haematology|December 21, 2000
Phenotypic and molecular diversity of haemoglobin H disease: a Greek experienceE Kanavakis, I Papassotiriou, M Karagiorga, et al.
British Journal of Haematology|February 1, 1996
The interaction of alpha zero thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy HE Kanavakis, J Traeger-Synodinos, I Papasotiriou, et al.
Clinical Genetics|February 17, 2015
Dysmorphology services: a snapshot of current practices and a vision for the futureS Douzgou, E Chervinsky, Y Gyftodimou, et al.
Genetic Testing|February 24, 2001
Delineation of the spectrum of Wilson disease mutations in the Greek population and the identification of six novel mutationsG Loudianos, M Lovicu, P Solinas, et al.
American Journal of Human Genetics|November 1, 1983
Association of two DNA polymorphisms in the alpha-globin gene cluster: implications for genetic analysisJ S Wainscoat, D R Higgs, E Kanavakis, et al.
American Journal of Medical Genetics. Part A|June 25, 2010
De novo interstitial duplication of the 15q11.2-q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literatureSophia Kitsiou-Tzeli, Maria Tzetis, Christalena Sofocleous, et al.
Human Mutation|September 27, 2002
Abnormal mRNA splicing resulting from consensus sequence splicing mutations of ATP7BG Loudianos, M Lovicu, V Dessi, et al.
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