Beckwith-Wiedemann spectrum exhibiting a 46,XY karyotype caused by genome-wide paternal uniparental heterodisomy: a case report.

Hara S, Sato T, Shimokawa O, Pooh R, Watanabe Y, Kubiura-Ichimaru M, Soejima H.

Open source

DOI: 10.1186/s40246-026-01009-7
Published: 2026-06-23
Container: Hum Genomics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1186/s40246-026-01009-7,
  title = {Beckwith-Wiedemann spectrum exhibiting a 46,XY karyotype caused by genome-wide paternal uniparental heterodisomy: a case report.},
  author = {Hara S and  Sato T and  Shimokawa O and  Pooh R and  Watanabe Y and  Kubiura-Ichimaru M and  Soejima H.},
  year = {2026},
  journal = {Hum Genomics},
  doi = {10.1186/s40246-026-01009-7},
  url = {https://doi.org/10.1186/s40246-026-01009-7}
}

RIS

TY  - JOUR
TI  - Beckwith-Wiedemann spectrum exhibiting a 46,XY karyotype caused by genome-wide paternal uniparental heterodisomy: a case report.
AU  - Hara S
AU  -  Sato T
AU  -  Shimokawa O
AU  -  Pooh R
AU  -  Watanabe Y
AU  -  Kubiura-Ichimaru M
AU  -  Soejima H.
PY  - 2026
JO  - Hum Genomics
DO  - 10.1186/s40246-026-01009-7
UR  - https://doi.org/10.1186/s40246-026-01009-7
ER  -

APA

S, H., T, S., O, S., R, P., Y, W., M, K., & H., S. (2026). Beckwith-Wiedemann spectrum exhibiting a 46,XY karyotype caused by genome-wide paternal uniparental heterodisomy: a case report.. Hum Genomics. https://doi.org/10.1186/s40246-026-01009-7

Source records

europe-pmc · retrieved 2026-09-27T02:30:53.794Z
doaj · retrieved 2026-09-27T02:30:53.794Z