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Repository of UOI "Olympias"
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Author
6
Syrrou, M.
5
Lolis, D.
4
Pagoulatos, G.
4
Patsalis, P. C.
3
Bourantas, K. L.
3
Seferiadis, K.
2
Alamanos, Y.
2
Kranas, V.
2
Zikopoulos, K.
1
Anastasiadou, V.
.
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2
*Trinucleotide Repeats
2
Aged
2
Alleles
2
Child, Preschool
2
Chromosome Mapping
2
Fragile X Mental Retardation Protein
2
Fragile X Syndrome/*genetics
2
Genotype
2
Infant, Newborn
2
Mutation
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ΑΠΟΘΕΤΗΡΙΟ "ΟΛΥΜΠΙΑΣ"
ΨΗΦΙΑΚΗ ΒΙΒΛΙΟΘΗΚΗ "Ηπειρομνήμων"
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Quantitation of HBF gamma-chain types by HPLC in patients with myelodysplastic syndrome (Journal article)
Variation in the number of FMR1 microsatellite repeats in three subgroups of the Hellenic population (Journal article)
Prenatal diagnosis of beta-thalassaemia by coelocentesis (Journal article)
Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability (Journal article)
Seckel syndrome in a family with three affected children and hematological manifestations associated with chromosome instability (Journal article)
FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population (Journal article)
Genotypes of N-acetyltransferase-2 and risk of bladder cancer: a case-control study (Journal article)
Gamma-chain heterogeneity in Greek (delta beta)zero-thalassemia (Journal article)
Chromomycin A3-staining as an indicator of protamine deficiency and fertilization (Journal article)
Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus (Journal article)