Molecular characterization of imprinting disorders: Beckwith-Wiedemann, Silver-Russell, and Prader-Willi syndromes in Egyptian patients.

Mohamed AM, Eid O, Farid M, Ashaat E, Abdel-Salam GMH, El-Bassyouni HT, Essa M, Mahrous R, Erian PSF, Refaat KM, Fayez A, Zaki M

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DOI: 10.1186/s12887-025-05901-4
Published: 2025 Jul 29
Container: BMC pediatrics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1186/s12887-025-05901-4,
  title = {Molecular characterization of imprinting disorders: Beckwith-Wiedemann, Silver-Russell, and Prader-Willi syndromes in Egyptian patients.},
  author = {Mohamed AM and Eid O and Farid M and Ashaat E and Abdel-Salam GMH and El-Bassyouni HT and Essa M and Mahrous R and Erian PSF and Refaat KM and Fayez A and Zaki M},
  year = {2025},
  journal = {BMC pediatrics},
  doi = {10.1186/s12887-025-05901-4},
  url = {https://doi.org/10.1186/s12887-025-05901-4}
}

RIS

TY  - JOUR
TI  - Molecular characterization of imprinting disorders: Beckwith-Wiedemann, Silver-Russell, and Prader-Willi syndromes in Egyptian patients.
AU  - Mohamed AM
AU  - Eid O
AU  - Farid M
AU  - Ashaat E
AU  - Abdel-Salam GMH
AU  - El-Bassyouni HT
AU  - Essa M
AU  - Mahrous R
AU  - Erian PSF
AU  - Refaat KM
AU  - Fayez A
AU  - Zaki M
PY  - 2025
JO  - BMC pediatrics
DO  - 10.1186/s12887-025-05901-4
UR  - https://doi.org/10.1186/s12887-025-05901-4
ER  -

APA

AM, M., O, E., M, F., E, A., GMH, A., HT, E., M, E., R, M., PSF, E., KM, R., A, F., & M, Z. (2025). Molecular characterization of imprinting disorders: Beckwith-Wiedemann, Silver-Russell, and Prader-Willi syndromes in Egyptian patients.. BMC pediatrics. https://doi.org/10.1186/s12887-025-05901-4

Source records

pubmed · retrieved 2026-09-25T12:50:42.810Z