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I Georgiou

Showing results (1-10 of 93) with videos related to

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European Journal of Endocrinology|November 30, 2002
The genetic basis of polycystic ovary syndromeN Xita, I Georgiou, A Tsatsoulis
Human Genetics|July 2, 2005
Gene symbol: SLC3A1. Disease: CystinuriaA Chatzikyriakidou, N Sofikitis, I Georgiou
Ginekologia Polska|November 14, 1998
The thalassemia syndromes and pregnancy, molecular basis, clinical aspects, prenatal diagnosisR Najdecki, I Georgiou, D Lolis
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: SLC3A1. Disease: CystinuriaAnthoula Chatzikyriakidou, K D Kollios, I Georgiou
Acta Haematologica|January 1, 1994
Fetal globin stimulation during a short-term trial of erythropoietin in HbS/beta-thalassemia patientsK L Bourantas, I Georgiou, K Seferiadis
Haematologica|July 1, 1991
Quantitation of HBF gamma-chain types by HPLC in patients with myelodysplastic syndromeK L Bourantas, I Georgiou, K Seferiadis
Molecular Human Reproduction|May 10, 2005
Association of SHBG gene polymorphism with menarcheN Xita, A Tsatsoulis, I Stavrou, et al.
European Journal of Neurology|November 26, 2009
Paraoxonase gene polymorphisms and stroke severityL Lazaros, S Markoula, A Kyritsis, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Seckel syndrome in a family with three affected children and hematological manifestations associated with chromosome instabilityM Syrrou, I Georgiou, M Paschopoulos, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|June 1, 1995
High HbF in pregnancy is associated with the Xmn I polymorphism at the -158bp of the G gamma-globin geneD Lolis, I Georgiou, P Loizou, et al.
Pageof 10

Showing results (1-10 of 93) with videos related to

Sort By:
Pageof 10
European Journal of Endocrinology|November 30, 2002
The genetic basis of polycystic ovary syndromeN Xita, I Georgiou, A Tsatsoulis
Human Genetics|July 2, 2005
Gene symbol: SLC3A1. Disease: CystinuriaA Chatzikyriakidou, N Sofikitis, I Georgiou
Ginekologia Polska|November 14, 1998
The thalassemia syndromes and pregnancy, molecular basis, clinical aspects, prenatal diagnosisR Najdecki, I Georgiou, D Lolis
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: SLC3A1. Disease: CystinuriaAnthoula Chatzikyriakidou, K D Kollios, I Georgiou
Acta Haematologica|January 1, 1994
Fetal globin stimulation during a short-term trial of erythropoietin in HbS/beta-thalassemia patientsK L Bourantas, I Georgiou, K Seferiadis
Haematologica|July 1, 1991
Quantitation of HBF gamma-chain types by HPLC in patients with myelodysplastic syndromeK L Bourantas, I Georgiou, K Seferiadis
Molecular Human Reproduction|May 10, 2005
Association of SHBG gene polymorphism with menarcheN Xita, A Tsatsoulis, I Stavrou, et al.
European Journal of Neurology|November 26, 2009
Paraoxonase gene polymorphisms and stroke severityL Lazaros, S Markoula, A Kyritsis, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Seckel syndrome in a family with three affected children and hematological manifestations associated with chromosome instabilityM Syrrou, I Georgiou, M Paschopoulos, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|June 1, 1995
High HbF in pregnancy is associated with the Xmn I polymorphism at the -158bp of the G gamma-globin geneD Lolis, I Georgiou, P Loizou, et al.
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