Prenatal Diagnosis and Genotype-Phenotype Correlation in 8q21.11 Microdeletion Syndrome: A Case Report

Francesco Libotte, Katia Margiotti, Marco Fabiani, Alvaro Mesoraca, Claudio Giorlandino

Open source

DOI: 10.2147/imcrj.s542044
Published: 2026-02
Container: International Medical Case Reports Journal
Publisher: Informa UK Limited
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.2147/imcrj.s542044,
  title = {Prenatal Diagnosis and Genotype-Phenotype Correlation in 8q21.11 Microdeletion Syndrome: A Case Report},
  author = {Francesco Libotte and Katia Margiotti and Marco Fabiani and Alvaro Mesoraca and Claudio Giorlandino},
  year = {2026},
  journal = {International Medical Case Reports Journal},
  doi = {10.2147/imcrj.s542044},
  url = {https://doi.org/10.2147/imcrj.s542044}
}

RIS

TY  - JOUR
TI  - Prenatal Diagnosis and Genotype-Phenotype Correlation in 8q21.11 Microdeletion Syndrome: A Case Report
AU  - Francesco Libotte
AU  - Katia Margiotti
AU  - Marco Fabiani
AU  - Alvaro Mesoraca
AU  - Claudio Giorlandino
PY  - 2026
JO  - International Medical Case Reports Journal
DO  - 10.2147/imcrj.s542044
UR  - https://doi.org/10.2147/imcrj.s542044
ER  -

APA

Libotte, F., Margiotti, K., Fabiani, M., Mesoraca, A., & Giorlandino, C. (2026). Prenatal Diagnosis and Genotype-Phenotype Correlation in 8q21.11 Microdeletion Syndrome: A Case Report. International Medical Case Reports Journal. https://doi.org/10.2147/imcrj.s542044

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crossref · retrieved 2026-09-26T11:21:26.223Z