Prenatal diagnosis of a familial 2p16.3 deletion encompassing NRXN1 associated with no apparently phenotypic abnormality in the family carrier members
- DOI
- 10.1016/j.tjog.2026.07.009
- Published
- 2026-09
- Container
- Taiwanese Journal of Obstetrics and Gynecology
- Publisher
- Elsevier BV
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.tjog.2026.07.009,
title = {Prenatal diagnosis of a familial 2p16.3 deletion encompassing NRXN1 associated with no apparently phenotypic abnormality in the family carrier members},
author = {Chih-Ping Chen},
year = {2026},
journal = {Taiwanese Journal of Obstetrics and Gynecology},
doi = {10.1016/j.tjog.2026.07.009},
url = {https://doi.org/10.1016/j.tjog.2026.07.009}
}RIS
TY - JOUR TI - Prenatal diagnosis of a familial 2p16.3 deletion encompassing NRXN1 associated with no apparently phenotypic abnormality in the family carrier members AU - Chih-Ping Chen PY - 2026 JO - Taiwanese Journal of Obstetrics and Gynecology DO - 10.1016/j.tjog.2026.07.009 UR - https://doi.org/10.1016/j.tjog.2026.07.009 ER -
APA
Chen, C. (2026). Prenatal diagnosis of a familial 2p16.3 deletion encompassing NRXN1 associated with no apparently phenotypic abnormality in the family carrier members. Taiwanese Journal of Obstetrics and Gynecology. https://doi.org/10.1016/j.tjog.2026.07.009
Source records
- crossref · retrieved 2026-09-27T13:18:02.820Z