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Publications by E Kanavakis
CLINICAL AND HEMATOLOGICAL PHENOTYPE IN 9 FAMILIES WITH THE RARE Β-Gene C>G MUTATION AT Nt POSITION 6 3′ TO THE TERMINATION CODON. 119
Pediatric Research
Child Health
Pediatrics
Perinatology
Phenotype-Genotype Correlation of Haemoglobinopathy H Disease in Greece 31
Pediatric Research
Child Health
Pediatrics
Perinatology
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Identification of a Novel Mutation in the Β-Globin Gene 3′ Untranslated Region [+1,506 (A>C)] in a Japanese Male With a Heterozygous Β-Thalassemia Phenotype
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Premature Termination Codon Mutations in the Von Willebrand Factor Gene Are Associated With Allele-Specific and Position-Dependent mRNA Decay
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Rare TACI Mutation in a 3-Year-Old Boy With CVID Phenotype
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A Premature-Termination Mutation in the Mus Musculus Cyclin-Dependent Kinase 3 Gene
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