Editorial: Fetal phenotypes of rare diseases: application and evaluation of prenatal exome sequencing and pathogenesis research of rare diseases

Front Genet. 2023 May 9:14:1205726. doi: 10.3389/fgene.2023.1205726. eCollection 2023.

¹ Center for Medical Genetics, Guangdong Women and Children Hospital, Guangzhou, China.
² Universitätsmedizin Marburg-Campus Fulda, Fulda, Germany.
³ Wonder Sir, Shanghai, China.
⁴ Shandong Provincial Key Laboratory of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.
⁵ Department of Biological Sciences, National University of Singapore, Singapore, Singapore.

No abstract available

Keywords: exome sequencing; fetal abnormalities; phenotype [mesh]; prenetal diagnosis; rare disease (RD).

Publication types

This editorial was supported by the a project to YZ from Science and Technology Department of Guangdong Province (2022A1515220097).