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Author
3
Hatzi, E.
2
Lazaros, L.
2
Markoula, S.
2
Paraskevaidis, E.
2
Siamopoulou, A.
2
Siomou, E.
1
Alamanos, Y.
1
Costi, C. E.
1
Dalkalitsis, N.
1
Deltas, C. C.
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Humans
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Case-Control Studies
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DNA Mutational Analysis
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Infant
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Kidney/*abnormalities
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Polymorphism, Genetic
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Date
1
2010 - 2011
7
2000 - 2009
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ΑΠΟΘΕΤΗΡΙΟ "ΟΛΥΜΠΙΑΣ"
ΨΗΦΙΑΚΗ ΒΙΒΛΙΟΘΗΚΗ "Ηπειρομνήμων"
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Results 1-8 of 8 (Search time: 0.649 seconds).
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Non-invasive first-trimester detection of paternal beta-globin gene mutations and polymorphisms as predictors of thalassemia risk at chorionic villous sampling (Journal article)
Novel PKD1 deletions and missense variants in a cohort of Hellenic polycystic kidney disease families (Journal article)
Non-invasive prenatal detection of paternal origin hb lepore in a male fetus at the 7th week of gestation (Journal article)
Gender association of the angiotensin-converting enzyme gene with ischaemic stroke (Journal article)
Impact of renin-angiotensin-aldosterone system genes on the treatment response of patients with hypertension and metabolic syndrome (Journal article)
Glutathione S-transferase null genotypes in transitional cell bladder cancer: a case-control study (Journal article)
Angiotensin II type 2 receptor gene polymorphism in Caucasian children with a wide spectrum of congenital anomalies of the kidney and urinary tract (Journal article)
Absence of mutations in the HOXA11 and HOXD11 genes in children with congenital renal malformations (Journal article)