A Clinical Genetics-Driven Dual Diagnosis of Prader-Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL.

Bogliardi FM, D'Ambrosio P, Quattromini G, Di Mario G, Pomponi MG, Miele L, Vergani E, Zampino G, Liguori A, Zollino M, Crinò A

Open source

DOI: 10.3390/genes17080937
Published: 2026 Aug 11
Container: Genes
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.3390/genes17080937,
  title = {A Clinical Genetics-Driven Dual Diagnosis of Prader-Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL.},
  author = {Bogliardi FM and D'Ambrosio P and Quattromini G and Di Mario G and Pomponi MG and Miele L and Vergani E and Zampino G and Liguori A and Zollino M and Crinò A},
  year = {2026},
  journal = {Genes},
  doi = {10.3390/genes17080937},
  url = {https://doi.org/10.3390/genes17080937}
}

RIS

TY  - JOUR
TI  - A Clinical Genetics-Driven Dual Diagnosis of Prader-Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL.
AU  - Bogliardi FM
AU  - D'Ambrosio P
AU  - Quattromini G
AU  - Di Mario G
AU  - Pomponi MG
AU  - Miele L
AU  - Vergani E
AU  - Zampino G
AU  - Liguori A
AU  - Zollino M
AU  - Crinò A
PY  - 2026
JO  - Genes
DO  - 10.3390/genes17080937
UR  - https://doi.org/10.3390/genes17080937
ER  -

APA

FM, B., P, D., G, Q., G, D. M., MG, P., L, M., E, V., G, Z., A, L., M, Z., & A, C. (2026). A Clinical Genetics-Driven Dual Diagnosis of Prader-Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL.. Genes. https://doi.org/10.3390/genes17080937

Source records

pubmed · retrieved 2026-09-25T12:44:14.117Z