Prenatal diagnosis of a familial 19q13.42 microdeletion with a favorable fetal outcome and no apparently phenotypic abnormality in the family carrier members.
- DOI
- 10.1016/j.tjog.2026.07.007
- Published
- 2026 Sep
- Container
- Taiwanese journal of obstetrics & gynecology
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.tjog.2026.07.007,
title = {Prenatal diagnosis of a familial 19q13.42 microdeletion with a favorable fetal outcome and no apparently phenotypic abnormality in the family carrier members.},
author = {Chen CP},
year = {2026},
journal = {Taiwanese journal of obstetrics \& gynecology},
doi = {10.1016/j.tjog.2026.07.007},
url = {https://doi.org/10.1016/j.tjog.2026.07.007}
}RIS
TY - JOUR TI - Prenatal diagnosis of a familial 19q13.42 microdeletion with a favorable fetal outcome and no apparently phenotypic abnormality in the family carrier members. AU - Chen CP PY - 2026 JO - Taiwanese journal of obstetrics & gynecology DO - 10.1016/j.tjog.2026.07.007 UR - https://doi.org/10.1016/j.tjog.2026.07.007 ER -
APA
CP, C. (2026). Prenatal diagnosis of a familial 19q13.42 microdeletion with a favorable fetal outcome and no apparently phenotypic abnormality in the family carrier members.. Taiwanese journal of obstetrics & gynecology. https://doi.org/10.1016/j.tjog.2026.07.007
Source records
- pubmed · retrieved 2026-09-25T17:48:08.498Z