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Case report: Prenatal diagnosis of fetal intracranial hemorrhage due to compound mutations in the JAM3 gene.
Xu, Min; Jin, Pengzhen; Huang, Yingzhi; Qian, Yeqing; Lin, Miaochun; Zuo, Juan; Zhu, Jin; Li, Zhaohui; Dong, Minyue.
Affiliation
  • Xu M; Laboratory of Prenatal Diagnosis, Mindong Hospital Affiliated to Fujian Medical University, Ningde, China.
  • Jin P; Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
  • Huang Y; Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
  • Qian Y; Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
  • Lin M; Laboratory of Prenatal Diagnosis, Mindong Hospital Affiliated to Fujian Medical University, Ningde, China.
  • Zuo J; Laboratory of Prenatal Diagnosis, Mindong Hospital Affiliated to Fujian Medical University, Ningde, China.
  • Zhu J; Laboratory of Prenatal Diagnosis, Mindong Hospital Affiliated to Fujian Medical University, Ningde, China.
  • Li Z; Laboratory of Prenatal Diagnosis, Mindong Hospital Affiliated to Fujian Medical University, Ningde, China.
  • Dong M; Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Front Genet ; 13: 1036231, 2022.
Article in En | MEDLINE | ID: mdl-36339007
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Prognostic_studies Language: En Journal: Front Genet Year: 2022 Document type: Article Affiliation country: China
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Prognostic_studies Language: En Journal: Front Genet Year: 2022 Document type: Article Affiliation country: China