OMIX

Prenatal Diagnosis of Fetal Intracranial Hemorrhage due to Compound Mutations in the JAM3 Gene

OMIX001498

1Summary
Title Prenatal Diagnosis of Fetal Intracranial Hemorrhage due to Compound Mutations in the JAM3 Gene
Description Intracranial hemorrhage is occasionally identified in fetus, whose genetic causes are greatly underestimated. In our investigation, three consecutive fetal intracranial hemorrhage were identified. The pathogenic variants of c.712+2T>A and c.813C>G in the JAM3 gene were proven to be its genetic causes.
Organism Homo
Data Type Magnetic Resonance Imaging (MRI)
Data Accessibility Controlled-access
BioProject PRJCA010990
Release Date 2023-12-30
Submitter Minyue Dong (dongmy@zju.edu.cn)
Organization Women's hospital, School of Medicine, Zhejiang University
Submission Date 2022-08-04
2Files & Download

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File ID File Title Number/Samples File Type File Size File Suffix Download Times Download
OMIX001498-02 MRI 1 Magnetic Resonance Imaging (MRI) 1.9 MB zip 0 Controlled

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