Experts

Name Expertise Affiliation Country ITHANET contributions
Elen NastasChief of Centre of Haemoglobinopathies - Paediatrics/Haematology Haemoglobinopathies Institute of PediatricsAlbaniaNo
Jim VadolasHaemoglobinopathies, gene therapy, HbF inductionRoyal Children's HospitalAustraliaNo
Beatrice GulbisHereditary red blood cell disordersi.e. red blood cell enzymes, membranopathies and haemoglobinopathies: phenotype including neoanal screening for haemoglobinopathies, genotype and genetic counselling Hôpital ErasmeBelgiumNo
Nicola ConranSickle cell disease University of Campinas BrazilNo
Denka Hrystova StoyanovaHematologist, thalassaemia patients treatmentSpecialized Children's Oncohematology HospitalBulgariaNo
Michael Angastiniotisthalassaemia, epidemiologyThalassaemia International FederationCyprusIthaMaps
George ChristopoulosHaemoglobinopathies, Prenatal Diagnosis, Preimplantation Genetic DiagnosisThe Cyprus Institute of Neurology and GeneticsCyprusNo
Soteroula ChristouDiagnosis of Haemoglobinopathies, Management of β-thalassemia, H-Disease, Sickle Cell Disease. Research interest in Treatment of β-thalasaemia (chelation, increase of Hb-F), Gene TherapyArchbishop Makarios Hospital IIICyprusNo
Xenia FelekiHaemoglobinopathies, prenatal diagnosisThe Cyprus Institute of Neurology and GeneticsCyprusNo
Michael HadjigabrielHaemoglobinopathy patients treatmentLimassol General HospitalCyprusNo
Georgia HatzilambiHaemoglobinopathies, population carrier screeningArchbishop Makarios Hospital IIICyprusNo
Christiana IoannouThalassaemia carrier screeningArchbishop Makarios Hospital IIICyprusNo
Eleni KaritzieHaemoglobinopathies, prenatal diagnosisThe Cyprus Institute of Neurology and GeneticsCyprusNo
Marina KleanthousDrug therapy for thalassaemia using HbF inducers, Gene therapy for thalassaemia, Development of a diagnostic chip for thalassaemia, Non-invasive prenatal diagnosis (NIPD) for thalassaemia, Studies on the molecular basis of different forms of thalassaemia The Cyprus Institute of Neurology and GeneticsCyprusIthaMaps
Annita KolnagouThalassaemia patient treatmentPaphos General HospitalCyprusNo
Andreani KyrriPopulation carrier screening for haemoglobinopathies. EpidemiologyArchbishop Makarios Hospital IIICyprusNo
Loukas KythreotisThalassaemia carrier screeningArchbishop Makarios Hospital IIICyprusNo
Carsten W. LedererGene Therapy, haemoglobinopathiesThe Cyprus Institute of Neurology and GeneticsCyprusIthaMaps, IthaPedia, IthaGenes
Christiana MakariouThalassaemia carrier screeningArchbishop Makarios Hospital IIICyprusNo
Natalia MichaelidouMember of patient associationPancyprian Thalassaemia AssociationCyprusNo
Evdokia PangalouHaematology, haemoglobinopathies patient treatmentArchbishop Makarios Hospital IIICyprusNo
Thessalia PapasavvaHaemoglobinopathies, prenatal diagnosis, non invasive prenatal diagnosisThe Cyprus Institute of Neurology and GeneticsCyprusNo
Eleni PavlouHaemoglobinopathies, diagnosis, prenatal diagnosisThe Cyprus Institute of Neurology and GeneticsCyprusNo
Loizos PerickleousThalassaemia patient associationPancyprian Thalassaemia AssociationCyprusNo
Miranda PetrouHaemoglobinopathies, molecular genetics, prenatal diagnosisThe Cyprus Institute of Neurology and GeneticsCyprusNo
Marios Phylactideshaemoglobinopathies, HbF induction, genetic modifiersThe Cyprus Institute of Neurology and GeneticsCyprusNo
Irene SavvidouThalassaemia patients treatmentArchbishop Makarios Hospital IIICyprusNo
Krikor SimamonianCardiology, thalassaemiaArchbishop Makarios Hospital IIICyprusNo
Maria SitarouHaemoglobinopathy patients treatmentLarnaca General HospitalCyprusNo
Nikos Skordishaemoglobinopathies, EndocrinologyArchbishop Makarios Hospital IIICyprusNo
Ahmed VaroglouPatient association memberCyprusNo
Mustafa YazmanHamoglobinopathies, prenatal diagnosisThalassaemia Center (Turkish Cypriot)CyprusNo
Amal El BeshlawyHaemoglobinopathies patient care, thalassemia patient Association memberCairo UniversityEgyptNo
Ghada EzzatHaemoglobinopathiesFayoum UniversityEgyptNo
Samia TemtamyHaemoglobinopathies, geneticsNational Research CentreEgyptNo
Catherine Badensred cells genetic disorders, thalassaemiaHôpital La TimoneFranceIthaMaps
Patricia Aguilar Martinezred cell disorders, rare anaemias, thalassemia, hemoglobin disorders, iron overload, hemochromatosis, iron deficiency anemiaCentre Hospitalier Universitaire de MontpellierFranceNo
Henri WajcmanHaemoglobinopathies, haemoglobin variants, databasesInstitut national de la santé et de la recherche médicaleFranceIthaPedia
Nicholas Anagnougene therapyNational and Kapodistrian University of AthensGreeceNo
Aglaia AthanasiadouGene therapyUniversity of PatrasGreeceNo
Adamandia PapachatzopoulouGene therapyUniversity of PatrasGreeceNo
Ioannis GeorgiouScreening and prenatal diagnosis of thalassemias and hemoglobinopathies, Population genetics, Medical genetics, PND, fetal maternal medicine genetic screeningUniversity Hospital of IoanninaGreeceNo
Eleni HassapopoulouHematologist / Thalassemia / Sickle cell disease AHEPA University General Hospital of Thessaloniki GreeceNo
Emmanuel Kanavakis Clinical genetics and pediatrics, Clinical and molecular genetics, Preventive pediatrics, Pediatric hematology, Genetic councelingNational and Kapodistrian University of AthensGreeceIthaPedia
Eleni KatsantoniTranscriptional regulation, transcription factors, STATs, STAT5, erythropoietic transcription factors, thalassaemiaBiomedical Research Foundation of the Academy of AthensGreeceNo
Antonis KattamisPediatric Hematology-Oncology, Hemoglobinopathies, thalassemia, sickle cell anemia, Diamond-Blackfan anemia, neutropenia, bone marrow failure syndromes, rare anemias, aplastic anemia, iron disorders “Aghia Sophia” Children’s HospitalGreeceNo
Panagoula KoliaHaemoglobinopathiesNational and Kapodistrian University of AthensGreeceNo
Theodoros KosteasFunctional Genomics and AgingInstitute of Molecular Biology and BiotechnologyGreeceNo
Dimitris LoukopoulosThalassaemia patients treatmentLaiko General Hospital AthensGreeceNo
George PatrinosPharmacogeneticsUniversity of PatrasGreeceNo
Jan Traeger SynodinosMolecular Genetics, Molecular diagnostics, Molecular Methods, Prenatal Diagnosis, Preimplantation Genetic Diagnosis, Haemoglobinopathies, Thalassaemia, Reproductive GeneticsNational and Kapodistrian University of AthensGreeceIthaMaps, IthaGenes, IthaPedia
Varnavas KonstantinouGene therapyGeorge Papanicolaou HospitalGreeceNo
Ersi VoskaridouThalassaemia, Sickle cell patient's treatment. Population screening and Prenatal diagnosisLaiko General Hospital AthensGreeceIthaPedia, IthaMaps
Christina Vrettoudiagnosis of thalassaemia, prenatal diagnosis, Preimplantation genetic diagnosisNational and Kapodistrian University of AthensGreeceIthaPedia
Evangelia YannakiGene therapy of haemoglobinopathiesGeorge Papanicolaou HospitalGreeceNo
Renu SaxenaHaemoglobinopathies, molecular geneticsSir Ganga Ram HospitalIndiaNo
Hossein NajmabadiHaemoglobinopathies, prenatal diagnosisKariminejad & Najmabadi Pathology and Genetics CenterIranNo
Rasool Khalid LuqmanClinical Hematologist, Thalassemia, Hemophilia and Congenital Blood Disorders Hiwa Hematology Oncology HospitalIraqNo
Oppenheim AriellahaemoglobinopathiesThe Hebrew University of JerusalemIsraelNo
Eitan FibachThalassaemia. Erythroid cell culturesHadassah Medical CenterIsraelNo
Dvora FilonGenetic Modifiers in Beta-thalassemiaHadassah Medical CenterIsraelNo
Emanuele AngelucciHemoglobinopathies. Hemopoietic stem cell transplantation in not malignant and in malignant diseases. Iron chelation in MDSOspedale Oncologico di Riferimento Regionale "Armando Businco"ItalyNo
Clara CamaschellaProfessor of Internal Medicine, rare anaemias Università Vita-Salute San RaffaeleItalyNo
Maria Domenica CappelliniThalassemia Syndromes; Hemoglobinophaties; G6PD; Gaucher Disease; Fabry Disease; PorphyriasUniversity of MilanItalyNo
Giuseppe CurcioFondazione Europea per la Genetica European Genetics Foundation - EGF European Genetics FoundationItalyNo
Giuliana FerrariGene therapy for haemoglobinopathiesScientific Institute H.S.RaffaeleItalyNo
Renzo GalanellohaemoglobinopathiesThe University of CagliariItalyNo
Roberto GambariHaemoglobinopathies, HbF induction, Genetic modifiers Università degli Studi di Ferrara ItalyIthaPedia
Achille Iolasconanaemia, red blood cells, erythropoiesis, dyserythropoiesis, red cell membraneUniversity Federico II of NaplesItalyNo
Aurelio MaggioThalassemia and Haemoglobionopaties and Blood Disease, Genetic Rare Disease Ospedali Riuniti Villa Sofia-CervelloItalyIthaMaps
Paolo MoiHaemoglobinopathies, molecular diagnosis, HbF induction, genetic modifiersThe University of CagliariItalyIthaMaps
Andrea MoscaDept. Science and Biomedical Technology University of Milano University of MilanItalyNo
Antonio PigaThalassaemia patients treatmentUniversity of Turin ItalyNo
Christina Rosatellithalassaemia patients treatmentThe University of CagliariItalyNo
Franco LocatelliPediatric Hematology / Oncology IRCCS Policlinico San Matteo Policlinico "San Mateo" - Pavia Instituto di Ricovero e Cura a Carattere Scientifico Di Diritto Publico - Ispedale Generale Regionale Oncoematologia Pediatrica Direttore: Dott. Franco LocaPoliclinico San Matteo Pavia Fondazione IRCCSItalyNo
Hanan HamamyEpidemiology of congenital disorders, consanguinity, community genetics services University of GenevaSwitzerlandNo
Basma I. HasanJordanNo
Ayman Al QadoumiGenetics of thalassaemia King Hussein Medical Center JordanNo
Ali TaherHemoglobinopathies (Thalassemia and Sickle Cell), Hemophilia and rare bleeding disorders, ThrombophiliaAmerican University of Beirut Medical CenterLebanonNo
Joseph BorgHaemoglobinopathies, regulation of globin gene expressionUniversity of MaltaMaltaNo
Alex Feliceepidemiology, genetics and gene control of human haemoglobin and thalassaemia, human genetics, medical biotechnology University of MaltaMaltaNo
Piero GiordanoHaemoglobinopathies, molecular diagnosisLeiden University Medical CenterNetherlandsIthaPedia
Frank GrosveldRegulation of globin gene expressionErasmus Medical Center NetherlandsNo
Cornelis L. Harteveldhaemoglobinopathies, α-thalassemia, β-thalassemia, haemoglobin variants, MLPA, mutation detection, technology, diagnostics, array CGH, non-invasive prenatal diagnosis, deletions Leiden University Medical CenterNetherlandsIthaMaps, IthaGenes, IthaPedia
Sjaak PhilipsenRegulation of globin gene expression, erythropoiesisErasmus Medical Center NetherlandsNo
Leticia RibeiroRed blood cell diseases and iron metabolism disorders on their clinical and laboratory aspects. Congenital haemostasis disorders, haemoglobinopathiesCentro Hospitalar e Universitário de CoimbraPortugalIthaMaps
Ramin BadiiHaemoglobinopathies, molecular diagnosisHamad Medical CorporationQatarNo
Mashael Jamal Mohammed Al JabirMolecular Genetics, haemoglobinopathiesHamad Medical CorporationQatarNo
Letitia DanGenetics, haemoglobinopathiesUniversity of BucharestRomaniaNo
Rodica TalmaciDevelopment and research activity in Molecular Biology Laboratories, Molecular investigation of haematological malignancies, Molecular diagnosis of genetic diseases, Prenatal diagnosis of thalassemias, Gene mutation identificationUniversity of BucharestRomaniaNo
Ibtessam Husseinhaemoglobinopathies National Research CentreEgyptNo
Joan-LLuis Vives CorronsClinical haematology diagnosis, University teaching, Haematology laboratory, Standardization, External quality assessment, rare anaemias, erythroenzymopathies , haemoglobinopathies.Hospital Clínic de BarcelonaSpainIthaMaps
Maria del Mar Mañú PereiraRed Cell Pathology, Laboratory diagnosis: phenotype and genotype, Thalassemia syndromes, Sickle cell disease (SCD), Enzymopathies, Membranopathies, Neonatal screening for SCD, EpidemiologyEuropean Network for Rare and Congenital AnaemiasSpainNo
Florinda GilsanzHematology Hospital Universitario 12 de OctubreSpainNo
Ana Maria Villegasα-thalassemia, β-thalassemia, P50, Hemoglobinophaties, Iron overload, Iron quelation, RM Iron overload, PNHHospital Clinicico San CarlosSpainNo
Faizeh Al QuobailiHaemoglobinopathiesDamascus UniversitySyriaNo
Suthat Fucharoeanthalassemia, abnormal hemoglobinsMahidol UniversityThailandNo
Vip Viprakasithaemoglobinopathiy patients treatment, molecular geneticsMahidol UniversityThailandNo
Habiba Chaabounihaemoglobinopathies, genetic diseasesHopital Charles Nicolle TunisTunisiaNo
Slaheddine FattoumHaemoglobinopathies, molecular diagnosisHopital d' EnfantsTunisiaNo
Yeshim AydinokPaediatric Haematology, haemoglobinopathies Ege University TurkeyNo
A.Nazli BasakGenetics and molecular pathology of inherited Hb disorders, Molecular mechanisms leading to neurodegenerative diseases Bogazici University TurkeyNo
Duran CanatanPediatrics, Hematologist, Geneticisit, Blood Transfusion and Blood Banking. Hemoglobinopathies. Congenital Red Cell Membrane defectsMediterrranean Blood Diseases Foundation (Akdeniz Kan Hastalıkları Vakfı) Hemoglobinopathy Diagnosis CenterTurkeyNo
Erol BaysalThalassemia genotype/phenotype correlation, state-of-the-art lab diagnostics, regulation of the globin genes, new methodologies to detect rare gene arrangements, thalassemia treatment and management, fetal globin induction Senior lecturer Dubai MedicalDubai Medical College United Arab EmiratesNo
Michael AntoniouHaemoglobinopathies, gene therapyKing's College LondonUnited KingdomNo
Mathew Darlisonhaemoglobinopathies epidemiology, bioinformaticsUCL Centre for Health Informatics & Multiprofessional EducationUnited KingdomNo
Douglas HiggsDirector of the Molecular Haematology Unit and Hon. Consultant Haematologist, alpha thalassaemia, Bioinformatics, Chromosome mapping, Computational biology and In situ hybridisation John Radcliffe HospitalUnited KingdomNo
Bernadette ModellHaemoglobinopathies, Epidemiology, Emeritus Professor of Community Genetics, Primary Care & Population Health, Institute of Epidemiology & Health, Faculty of Pop Health SciencesUCL Institute of Epidemiology and Health CareUnited KingdomNo
John OldHaemoglobinopathies, prenatal diagnosis, epidemiologyChurchill HospitalUnited KingdomIthaGenes
Dudley PennellCardiac complications in thalassemia. Professor of Cardiology at the National Heart and Lung Institute. Director of the National Institutes of Health Research Cardiovascular Biomedical Research Unit located at Royal Brompton HospitalImperial College LondonUnited KingdomNo
Mary Petrouhaemoglobinopathies, prenatal diagnosisUCL Institute for Women's HealthUnited KingdomNo
John PorterBlood diseases, haemoglobinopathies John Porter is Professor of Haematology and Consultant Haematologist at the University College London Hospitals in London, UK and head of the joint Red Cell Unit for UCLH and Whittington HospitalsUniversity College London HospitalsUnited KingdomNo
Paul TelferHeamoglobinopathy patients treatmentRoyal London HospitalUnited KingdomNo
Swee Lay TheinHaemoglobinopathy patients treatment, regulation of globin gene expressionThe National Institutes of HealthUnited States of AmericaNo
Ross Hardisonregulation of globin gene expressionPSU Center for Comparative Genomics & BioinformaticsUnited States of AmericaNo
Abdullah KutlarHaemoglobinopathies, Hematology Georgia Regents UniversityUnited States of AmericaNo
Stefano RivellaKwame Ohene-Frempong Chair on Sickle Cell Anemia and Professor of Pediatrics; Erythropoiesis, iron metabolism, macrophages, gene therapy, iPS cellsThe Children's Hospital of PhiladelphiaUnited States of AmericaNo
Michel SadelainHaemoglobinopathies, gene therapy Memorial Sloan–Kettering Cancer CenterUnited States of AmericaNo
George StamatoyannopoulosHaemoglobinopathies, gene therapy, HbF induction, regulation of globin gene expressionUniversity of WashingtonUnited States of AmericaNo
Petros Kountourisbioinformatics, computational biology, haemoglobinopathiesThe Cyprus Institute of Neurology and GeneticsCyprusIthaGenes, IthaMaps, IthaPedia, IthaChrom
Lawrence FaulknerHaemoglobinopathies, Bone marrow transplantation Cure2ChildrenItalyNo
Mohamed El MissirythalassaemiaCure2ChildrenUnited States of AmericaNo
Frédéric PielEpidemiology of haemoglobinopathiesImperial College LondonUnited KingdomNo
Petr Holubthalassaemia, electronic infrastructureMasaryk UniversityCzech RepublicNo
Shaza AbusirryaHaemoglobinopathies, molecular diagnosisHamad Medical CorporationQatarNo
Paolo De CoppiIn utero stem cell therapyUCL Institute for Women's HealthUnited KingdomNo
Anna DavidIn utero stem cell therapyUCL Institute for Women's HealthUnited KingdomNo
Toni Cathomengene therapyUniversity of Freiburg - Albert-Ludwigs-Universität FreiburgGermanyNo
Panicos ShangarisIn utero stem cell therapyUCL Institute for Women's HealthUnited KingdomNo
Laura BredaResearch Assistant Professor; Gene therapyThe Children's Hospital of PhiladelphiaUnited States of AmericaNo
Valeriya KalevaHaemoglobinopathy patients treatment, thalassaemiaUniversity Hospital “St. Marina”BulgariaIthaMaps
Madeeha M. KamalHaematology, haemoglobinopathy patients treatmentHamad Medical CorporationQatarNo
Shirley HendersonHaemoglobinopathies, prenatal diagnosis Churchill HospitalUnited KingdomNo
Christian Scerri Thalassaemia patients treatment, thalassaemia geneticsUniversity of MaltaMaltaNo
Nicolas PilarEthical and Legal issuesThe University of the Basque CountrySpainNo
Mohammad HamidMolecular Genetics Molecular Medicine Biotechnology ResearchPasteur Institute of IranIranNo
Andrea ZanollaProject Manager European Genetics Foundation European Genetics FoundationItalyNo
Julia HoffmannProgramm Officer for Fund Raising European Genetics Foundation European Genetics FoundationItalyNo
Antonio CaoThalassaemia patient treatmentThe University of CagliariItalyNo
Emilio José Armaza ArmazaEthical, Legal and Social Implications (ELSI) in rare anaemias The University of Deusto SpainNo
Miguel AbboudPediatrics American University of BeirutLebanonNo
AbuAli Azhar Mohammed Abu AliSenior Clinical Psychologist Latifa Hospital Dubai Health Authority United Arab Emirates Latifa HospitalUnited Arab EmiratesNo
Abdullah Hussein Al-JeffriExecutive Director KFNCC Consultant Pediatric Hem/One King Faisal Specialist Hospital and Research Centre Saudi Arabia King Faisal Specialist Hospital & Research CentreSaudi ArabiaNo
Awatif Al BaharDGFC medical director Consultant in obstetrics, gynaecology and endocrine infertility Dubai Health Authority Head of Department of Obstetrics & Gynaecology Canadian Hospital United Arab Emirates Canadian Hospital United Arab EmiratesUnited Arab EmiratesNo
Azzam Al ZoebiConsultant Pediatric Hematologist-Oncologist Sheikh Khalifa Medical CityUnited Arab EmiratesNo
Eleni KalogerouPopulation screening for thalassaemiaArchbishop Makarios Hospital IIICyprusNo
Androulla EleftheriouhaemoglobinopathiesThalassaemia International FederationCyprusNo
Eleni PapanicolaouGene therapyNational and Kapodistrian University of AthensGreeceNo
Roswitha Dickerhoff Sickle cell anaemia and thalassaemia management and diagnosis, epidemiology of haemoglobinopathies in Germany, advocacy for the recognition of haemoglobinopathies in disease management and preventionUniversity Hospital Düsseldorf GermanyNo
Holger Cario HaemoglobinopathiesUlm University Medical CentreGermanyNo
Claudia Potthoff Department of Paediatric Oncology, Haematology and Clinical ImmunologyUniversity Hospital Düsseldorf GermanyNo
Elisabeth KohneHaemoglobinopathies diagnosisUlm University Medical CentreGermanyNo
Regine GrossePaediatric Haematology and Oncology University Hospital Hamburg-EppendorfGermanyNo
Maria del PilarSickle cell patientsMeharry Medical CollegeUnited States of AmericaNo
Deborah RundLeukemia, Thalassemia, Drugs resistance, hemapheresisHadassah Medical CenterIsraelNo
David Weatherallgenetic, adaptive and environmental factors that modify the phenotype of common forms of thalassaemia, population genetics of the thalassaemiasUniversity of OxfordUnited KingdomNo
Celeste BentoRed blood cell disorders, Hemoglobinopathies, Congenital Erythrocytosis, Molecular GeneticsCentro Hospitalar e Universitário de CoimbraPortugalIthaChrom, IthaMaps
Raj Ramesarhaemoglobinopathies, retinal degenerative disorders, genetic basis of the more complex yet common chronic disorders (e.g. hypertension)University of Cape TownSouth AfricaNo
Zilfalil bin Alwihaemoglobinopathies, medical genetics, thalassaemia, population geneticsUniversiti Sains MalaysiaMalaysiaIthaMaps
Mas Rina Wati Abdul HamidHuman Genetics, Cancer Genetics and Biology, ThalassaemiaUniversiti Brunei DarussalamBruneiIthaMaps
Léon Tshilolosickle cell diseaseCentre Hospitalier Mère-Enfant MONKOLEDemocratic Republic of the CongoIthaMaps
Bertha Ibarragenetics, human genetics, haematologyUniversidad de GuadalajaraMexicoIthaMaps
F. Javier Pereagenetics, human genetics, haematologyUniversidad de GuadalajaraMexicoNo
Salah Al-HumoodhaematopathologyKuwait UniversityKuwaitIthaMaps
Fahd Al-Mullahaemoglobin disordersKuwait UniversityKuwaitIthaMaps
Obiageli NnoduHaematology and blood transfusionSickle Cell Support Society of NigeriaNigeriaIthaMaps
Hafizur RahmanThalassaemia and haemoglobinopathies, chronic myeloid leukemia (CML)International Centre for Diarrhoeal Disease Research, BangladeshBangladeshIthaMaps
Pavlos Fanishaemoglobinopathies, globin regulationThe Cyprus Institute of Neurology and GeneticsCyprusIthaGenes
Joyce HarperJoyce Harper is Professor of Human Genetics and Embryology at the Institute for Women’s Health, University College London where she heads the Department of Reproductive Health and heads the Embryology, IVF and Reproductive Genetics GroupUCL Institute for Women's HealthUnited KingdomNo
Coralea Stephanouhaemoglobinopathies, gene therapy, medical genetics, molecular biologyThe Cyprus Institute of Neurology and GeneticsCyprusIthaChrom, IthaGenes, IthaMaps
Stephan LobitzSickle Cell Disease, HaemoglobinopathiesCharité - Universitätsmedizin BerlinGermanyNo

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