Prenatal Diagnosis of Fetal Intracranial Hemorrhage due to Compound Mutations in JAM3
| Title | Prenatal Diagnosis of Fetal Intracranial Hemorrhage due to Compound Mutations in JAM3 |
|---|---|
| Description | Intracranial hemorrhage is a common complication in preterm infants but occasionally identified in fetus. Disruptions of the genes are common genetic causes identified in the fetal intracranial hemorrhage, among which, the disruptions of the JAM3 gene are rarely reported. |
| Organism | Homo |
| Data Type | Other Type of Clinical information |
| Data Accessibility | Controlled-access |
| BioProject | PRJCA011485 |
| Release Date | 2023-12-31 |
| Submitter | Minyue Dong (dongmy@zju.edu.cn) |
| Organization | Women's hospital, School of Medicine, Zhejiang University |
| Submission Date | 2022-09-02 |
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| File ID | File Title | Number/Samples | File Type | File Size | File Suffix | Download Times | Download |
|---|---|---|---|---|---|---|---|
| OMIX001745-01 | Prenatal Diagnosis of Fetal Intracranial Hemorrhage due to Compound Mutations in the JAM3 Gene | 1 | Other Type of Clinical information | 1.9 MB | zip | 0 | Controlled |