# Seven cases of Wiedemann-Beckwith syndrome, including the first reported case of mosaic paternal isodisomy along the whole chromosome 11

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/seven-cases-of-wiedemann-beckwith-syndrome-including-the-first-reported-case-of/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Fabrizio Dutly,Alessandra Baumer,H�lya Kayserili,Memnune Y�ksel-Apak,Tatjana E. Zerova,Gundula Hebisch,Albert Schinzel |
| Citations | 63 |
| DOI | 10.1002/(sici)1096-8628(19981012)79:5<347::aid-ajmg4>3.0.co;2-g |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2067181161 |
| PMID | 9779800 |
| Type | article |
| Year | 1998 |

## Paper authors

- [Gundula Hebisch](https://scholariq.org/researchers/gundula-hebisch/)

## 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.