Clinical and genetic analysis of two phenotypically normal families carrying 4p16.1 microduplications
This paper highlights two families with clinically asymptomatic 4p16.1 microduplications that assisted in determining the pathogenicity of this fragment. The findings can be used as a reference for genetic counseling in cases of similar abnormalities encountered during future prenatal diagnosis.
Authors
- Xinqiang Lan (ORCID: https://orcid.org/0000-0002-4641-9910)
- Xiaolin L. Wang (ORCID: https://orcid.org/0000-0003-4150-0848)
- Yujiao Wang (ORCID: https://orcid.org/0000-0001-6860-1310)
Institutions
- Qingdao University (CN)
- Weihai Maternal and Child Health Hospital (CN)
Publication Details
- Journal
- Taiwanese Journal of Obstetrics and Gynecology
- Published
- 2024-09-01
- DOI
- https://doi.org/10.1016/j.tjog.2023.12.004
- Primary Topic
- Genomic variations and chromosomal abnormalities
- Type
- article
- Field-Weighted Citation Impact
- 0.00