Prenatal diagnosis of familial 8q24.11q24.12 and 8q24.13 microdeletions encompassing the exon 1 of EXT1 associated with no apparently phenotypic abnormality in the family carrier members.
- DOI
- 10.1016/j.tjog.2026.07.011
- Published
- 2026 Sep
- Container
- Taiwanese journal of obstetrics & gynecology
- Publisher
- Not recorded
- Open access
- no
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Cite this work
BibTeX
@article{allodium:10.1016/j.tjog.2026.07.011,
title = {Prenatal diagnosis of familial 8q24.11q24.12 and 8q24.13 microdeletions encompassing the exon 1 of EXT1 associated with 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.2026.07.011},
url = {https://doi.org/10.1016/j.tjog.2026.07.011}
}RIS
TY - JOUR TI - Prenatal diagnosis of familial 8q24.11q24.12 and 8q24.13 microdeletions encompassing the exon 1 of EXT1 associated with 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.2026.07.011 UR - https://doi.org/10.1016/j.tjog.2026.07.011 ER -
APA
CP, C. (2026). Prenatal diagnosis of familial 8q24.11q24.12 and 8q24.13 microdeletions encompassing the exon 1 of EXT1 associated with no apparently phenotypic abnormality in the family carrier members.. Taiwanese journal of obstetrics & gynecology. https://doi.org/10.1016/j.tjog.2026.07.011
Source records
- pubmed · retrieved 2026-09-27T13:19:02.096Z
- europe-pmc · retrieved 2026-09-27T13:19:02.117Z