## Abstract Angelman and PraderβWilli syndromes are clinically distinct neurobehavioral disorders most commonly resulting from large deletions of chromosome 15q11βq13. The deletions arise differentially during maternal or paternal gametogenesis, respectively. A subgroup of patients with either synd
β¦ LIBER β¦
Uniparental paternal disomy in Angelman's syndrome
β Scribed by Malcolm, S.; Clayton-Smith, J.; Nichols, M.; Pembrey, M.E.; Armour, J.A.L.; Jeffreys, A.J.; Robb, S.; Webb, T.
- Book ID
- 122522900
- Publisher
- The Lancet
- Year
- 1991
- Tongue
- English
- Weight
- 754 KB
- Volume
- 337
- Category
- Article
- ISSN
- 0140-6736
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