Satoshi Hara

2PUBLICATIONS
1CO-AUTHORS
Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)
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Publications (2)

|Jun 24, 2026
Beckwith-Wiedemann spectrum exhibiting a 46,XY karyotype caused by genome-wide paternal uniparental heterodisomy: a case report.

|Dec 02, 2024
Identification of responsible sequences which mutations cause maternal H19-ICR hypermethylation with Beckwith-Wiedemann syndrome-like overgrowth.

Satoshi Hara, Fumikazu Matsuhisa, Shuji Kitajima

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Frequent Collaborators

1 joint publications

Hidenobu Soejima