Genotype-phenotypic correlation in a Chinese patient with isolated lissencephaly sequence caused by 17p13.3p13.2 chromosomal microdeletion: a 6-year follow-up study.
- DOI
- 10.3389/fgene.2026.1866451
- Published
- 2026
- Container
- Frontiers in genetics
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3389/fgene.2026.1866451,
title = {Genotype-phenotypic correlation in a Chinese patient with isolated lissencephaly sequence caused by 17p13.3p13.2 chromosomal microdeletion: a 6-year follow-up study.},
author = {Tong J and Chen X and Wang T and Ma S and Zhao Y and Shi D and Wang X and Yan D},
year = {2026},
journal = {Frontiers in genetics},
doi = {10.3389/fgene.2026.1866451},
url = {https://doi.org/10.3389/fgene.2026.1866451}
}RIS
TY - JOUR TI - Genotype-phenotypic correlation in a Chinese patient with isolated lissencephaly sequence caused by 17p13.3p13.2 chromosomal microdeletion: a 6-year follow-up study. AU - Tong J AU - Chen X AU - Wang T AU - Ma S AU - Zhao Y AU - Shi D AU - Wang X AU - Yan D PY - 2026 JO - Frontiers in genetics DO - 10.3389/fgene.2026.1866451 UR - https://doi.org/10.3389/fgene.2026.1866451 ER -
APA
J, T., X, C., T, W., S, M., Y, Z., D, S., X, W., & D, Y. (2026). Genotype-phenotypic correlation in a Chinese patient with isolated lissencephaly sequence caused by 17p13.3p13.2 chromosomal microdeletion: a 6-year follow-up study.. Frontiers in genetics. https://doi.org/10.3389/fgene.2026.1866451
Source records
- pubmed · retrieved 2026-09-25T05:04:55.972Z