Case Report: From imaging to genetics: a case of congenital restrictive strabismus with SEOM expands the 22q11.2 duplication syndrome phenotype

Xingyuan Wei, Ruxin Gao, Renyi Xie

Open source

DOI: 10.3389/fmed.2026.1782101
Published: 2026-02-23
Container: Frontiers in Medicine
Publisher: Frontiers Media SA
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.3389/fmed.2026.1782101,
  title = {Case Report: From imaging to genetics: a case of congenital restrictive strabismus with SEOM expands the 22q11.2 duplication syndrome phenotype},
  author = {Xingyuan Wei and Ruxin Gao and Renyi Xie},
  year = {2026},
  journal = {Frontiers in Medicine},
  doi = {10.3389/fmed.2026.1782101},
  url = {https://doi.org/10.3389/fmed.2026.1782101}
}

RIS

TY  - JOUR
TI  - Case Report: From imaging to genetics: a case of congenital restrictive strabismus with SEOM expands the 22q11.2 duplication syndrome phenotype
AU  - Xingyuan Wei
AU  - Ruxin Gao
AU  - Renyi Xie
PY  - 2026
JO  - Frontiers in Medicine
DO  - 10.3389/fmed.2026.1782101
UR  - https://doi.org/10.3389/fmed.2026.1782101
ER  -

APA

Wei, X., Gao, R., & Xie, R. (2026). Case Report: From imaging to genetics: a case of congenital restrictive strabismus with SEOM expands the 22q11.2 duplication syndrome phenotype. Frontiers in Medicine. https://doi.org/10.3389/fmed.2026.1782101

Source records

crossref · retrieved 2026-09-26T02:39:24.699Z