Preimplantation genetic testing for concurrent Meckel Syndrome and hereditary breast cancer in a Chinese family harboring a novel NPHP3 pathogenic variant and a canonical BRCA2 frameshift variant
- DOI
- 10.1590/1678-4685-gmb-2025-0063
- Published
- 2026
- Container
- Genetics and Molecular Biology
- Publisher
- FapUNIFESP (SciELO)
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1590/1678-4685-gmb-2025-0063,
title = {Preimplantation genetic testing for concurrent Meckel Syndrome and hereditary breast cancer in a Chinese family harboring a novel NPHP3 pathogenic variant and a canonical BRCA2 frameshift variant},
author = {Yiyuan Zhang and Xianjing Huang and Pingping Qiu and Hong Ji and Lu Ding and Xuemei He and Yingying Shi and Yanru Huang and Ping Li and Libin Mei},
year = {2026},
journal = {Genetics and Molecular Biology},
doi = {10.1590/1678-4685-gmb-2025-0063},
url = {https://doi.org/10.1590/1678-4685-gmb-2025-0063}
}RIS
TY - JOUR TI - Preimplantation genetic testing for concurrent Meckel Syndrome and hereditary breast cancer in a Chinese family harboring a novel NPHP3 pathogenic variant and a canonical BRCA2 frameshift variant AU - Yiyuan Zhang AU - Xianjing Huang AU - Pingping Qiu AU - Hong Ji AU - Lu Ding AU - Xuemei He AU - Yingying Shi AU - Yanru Huang AU - Ping Li AU - Libin Mei PY - 2026 JO - Genetics and Molecular Biology DO - 10.1590/1678-4685-gmb-2025-0063 UR - https://doi.org/10.1590/1678-4685-gmb-2025-0063 ER -
APA
Zhang, Y., Huang, X., Qiu, P., Ji, H., Ding, L., He, X., Shi, Y., Huang, Y., Li, P., & Mei, L. (2026). Preimplantation genetic testing for concurrent Meckel Syndrome and hereditary breast cancer in a Chinese family harboring a novel NPHP3 pathogenic variant and a canonical BRCA2 frameshift variant. Genetics and Molecular Biology. https://doi.org/10.1590/1678-4685-gmb-2025-0063
Source records
- crossref · retrieved 2026-09-26T14:20:55.609Z