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Chromosome 15 uniparental disomy is not frequent in Angelman syndrome.

Genetic imprinting has been implicated in the etiology of two clinically distinct but cytogenetically indistinguishable disorders--Angelman syndrome (AS) and Prader-Willi syndrome (PWS). This hypothesis is derived from two lines of evidence. First, while the molecular extents of de novo cytogenetic...

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Detaylı Bibliyografya
Asıl Yazarlar: Knoll, J H, Glatt, K A, Nicholls, R D, Malcolm, S, Lalande, M
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1991
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682763/
https://ncbi.nlm.nih.gov/pubmed/1985457
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