# An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/an-imprinted-gene-p57kip2-is-mutated-in-beckwith-wiedemann-syndrome/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Izuho Hatada,Hirofumi Ohashi,Yoshimitsu Fukushima,Yasuhiko Kaneko,Masahiro Inoue,Yosuke Komoto,Akira Okada,Sachiko Oh‐ishi,Akira Nabetani,Hiroko Morisaki,Masahiro Nakayama,Norio Niikawa,Tsunehiro Mukai |
| Citations | 385 |
| DOI | 10.1038/ng1096-171 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W1997820996 |
| PMID | 8841187 |
| Type | article |
| Year | 1996 |

## Paper authors

- [Yoshimitsu Fukushima](https://scholariq.org/researchers/yoshimitsu-fukushima/)

## Paper primary topic

- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)

## Paper topics

- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)
- [Prenatal Screening and Diagnostics](https://scholariq.org/topics/prenatal-screening-and-diagnostics/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.