[Clinical phenotype and genetic analysis of a rare case with 6p duplication and terminal deletion syndrome].
The abnormal phenotype of the child may be attributed to the 6p duplication and terminal deletion.
Authors
- Xuzhuo Zhang
- Yanhong Yu (ORCID: https://orcid.org/0000-0002-1652-201X)
- Jian Lu (ORCID: https://orcid.org/0000-0001-8796-4088)
- Ye Xia (ORCID: https://orcid.org/0000-0002-4749-3119)
- Hong Li (ORCID: https://orcid.org/0000-0001-6930-4772)
- Yingying Gao (ORCID: https://orcid.org/0000-0002-7123-5363)
- Juan Qiu
- Jingtian Lu
Institutions
- Shenzhen Maternity and Child Healthcare Hospital (CN)
Publication Details
- Journal
- PubMed
- Published
- 2024-09-10
- DOI
- https://doi.org/10.3760/cma.j.cn511374-20230802-00032
- Primary Topic
- Genomic variations and chromosomal abnormalities
- Type
- article
- Field-Weighted Citation Impact
- 0.00