404 - Page not found
The page you were looking for has been removed or has changed location.
To assist you in finding the relevant information, an overview of the complete website contents is presented below:
- Home page
- Clinical Genetics Division
- Cytogenetics Division
- Molecular Genetics Division
- Angelman Syndrome
- Familial Breast Cancer
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Early-Onset Torsion Dystonia
- Fragile X Syndrome
- Friedreich Ataxia
- Osteogenesis Imperfecta Type VIII
- Hereditary non-Polyposis Colon Cancers
- Huntington Disease
- Prader Willi Syndrome
- Russell Silver Syndrome & primordial growth retardation
- Progressive familial intrahepatic cholestasis type 1
- Spinal Muscular Atrophy
- Uniparental disomy
- Research Projects
- The Molecular Genetics of Male Infertility.
- The Contribution of Cystic Fibrosis Mutations to Male Infertility.
- Molecular Genetics of Hereditary Breast Cancer in Ireland.
- European Molecular Genetics Quality Network - EMQN.
- Certified Reference Materials for Genetic Testing - CRMGEN.
- Investigation of the Genetic Basis of Vesicoureteral Reflux.
- Molecular Cytogenetic Studies of Neuroblastoma.
- Molecular Cytogenetic Studies of Leukaemogenesis.
- Genetic Susceptibility in the Irish Amyotrophic Lateral Sclerosis Population.
- Links
- Contact Us
- Publications