Case report: Prenatal diagnosis of fetal intracranial hemorrhage due to compound mutations in the JAM3 gene

Intracranial hemorrhage is a common complication in preterm infants but occasionally occurs in fetuses. Disruptions of the genes, such as the COL4A1 and COL4A2 genes, are common genetic causes identified in fetal intracranial hemorrhage; however, the disruptions of the JAM3 gene are rarely reported....

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Detalles Bibliográficos
Autores principales: Xu, Min, Jin, Pengzhen, Huang, Yingzhi, Qian, Yeqing, Lin, Miaochun, Zuo, Juan, Zhu, Jin, Li, Zhaohui, Dong, Minyue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9629614/
https://www.ncbi.nlm.nih.gov/pubmed/36339007
http://dx.doi.org/10.3389/fgene.2022.1036231

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9629614/
https://www.ncbi.nlm.nih.gov/pubmed/36339007
http://dx.doi.org/10.3389/fgene.2022.1036231

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