Genetic Diseases, Inborn: all 422 studies
Page 5 of 5. Open to participants first (147), then studies with results posted, then the rest; newest registration first within each.
- Investigation of Genetic Disease Marker Associated With Korean Glaucoma PatientsCompletedNCT01025024
- Observational Prospective Study on Patients Treated With Norditropin®CompletedNCT00960128
- Genetic Disease Gene IdentificationTerminatedNCT00916903
- Screening Protocol for Genetic Diseases of Allergic InflammationCompletedNCT00852943
- Fundus Changes in the Microphthalmy EyesCompletedNCT00811512
- Unrelated Hematopoietic Stem Cell Transplantation(HSCT) for Genetic Diseases of Blood CellsCompletedNCT00730314Phase 1/2
- Retrospective Observational Study on Efficacy and Safety of Norditropin® in Children With Prader-Willi SyndromeCompletedNCT00705172
- Face Anthropometric Pattern Recognition Technology for Computer Aided Diagnosis of Human Genetic Disorders.CompletedNCT00705055
- Allogeneic Bone Marrow Transplantation for the Treatment of Genetic Disorders of ErythropoiesisCompletedNCT00578435Phase 2
- Longitudinal Study of Genetic Causes of Intrahepatic Cholestasis (LOGIC)SuspendedNCT00571272
- High-Density Lipoprotein (HDL) Treatment StudyCompletedNCT00458055Not applicable
- Genetic Studies in the Amish and MennonitesCompletedNCT00359580
- Genetic Studies of X-linked Lymphoproliferative DiseaseCompletedNCT00359411
- Rare Genetic Disorders of the Breathing AirwaysCompletedNCT00323167
- Development of New Prenatal Diagnostic Tests From Maternal BloodTerminatedNCT00314691Not applicable
- Recombinant Human C1 Inhibitor for the Treatment of Acute Attacks in Patients With Hereditary AngioedemaCompletedNCT00262288Phase 2/3
- Recombinant Human C1 Inhibitor for the Treatment of Acute Attacks in Patients With Hereditary AngioedemaCompletedNCT00261053Phase 2
- Reproducibility of the Array-Based Comparative Genomic Hybridization (aCGH) System Using Whole Blood SamplesStatus unknownNCT00214448
- New York Blood Center National Cord Blood ProgramTerminatedNCT00212407Early Phase 1
- Studies of Children With Metabolic and Other Genetic DisordersCompletedNCT00025870
- Microarray Analysis for Human Genetic DiseaseCompletedNCT00001898
- Study of Clinical and Molecular Manifestations of Genetic DisordersCompletedNCT00001466