[Prenatal phenotype and genetic analysis of two fetuses with Bardet-Biedl syndrome].
Two rare fetuses with Bardet-Biedl syndrome have been diagnosed. Above finding has expanded the mutational spectrum of this syndrome and has important implications for genetic counseling for the affected families.
Authors
- Lingyi Zhang (ORCID: https://orcid.org/0000-0003-1690-578X)
- Xingguang Wang (ORCID: https://orcid.org/0000-0002-0520-4980)
- Yanyan Li (ORCID: https://orcid.org/0009-0005-7231-9293)
- Zhigang Zhang (ORCID: https://orcid.org/0009-0004-9603-1641)
Institutions
- People's Hospital of Cangzhou (CN)
Publication Details
- Journal
- PubMed
- Published
- 2025-02-10
- DOI
- https://doi.org/10.3760/cma.j.cn511374-20241019-00545
- Primary Topic
- Genetic and Kidney Cyst Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00