Whole genomic ( DrugBank: - )
1 disease
| 告示番号 | 疾患名（ページ内リンク） | 臨床試験数 |
|---|---|---|
| 285 | ファンコニ貧血 | 1 |
285. ファンコニ貧血
臨床試験数 : 62 / 薬物数 : 93 - (DrugBank : 30) / 標的遺伝子数 : 30 - 標的パスウェイ数 : 144
| No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | NCT01995305 (ClinicalTrials.gov) | October 2013 | 21/11/2013 | Use Massive Parallel Sequencing and Exome Capture Technology to Sequence the Exome of Fanconi Anemia Children and Their Patents | Exome Sequencing of Fanconi Anemia Children and the Their Parents | Fanconi Anemia;Autosomal or Sex Linked Recessive Genetic Disease;Bone Marrow Hematopoiesis Failure, Multiple Congenital Abnormalities, and Susceptibility to Neoplastic Diseases.;Hematopoiesis Maintainance. | Genetic: human whole exome;Genetic: whole genomic | Xiaofan Zhu | NULL | Available | 1 Month | 18 Years | Both | N/A | China |