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The Paradox of Prader Willi Syndrome: A genetic model of starvation

✍ Scribed by A. J. Holland


Book ID
114741149
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
44 KB
Volume
52
Category
Article
ISSN
0964-2633

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A genetic model for the Prader-Willi syn
✍ Ingo Kennerknecht πŸ“‚ Article πŸ“… 1992 πŸ› Springer 🌐 English βš– 944 KB

Sporadic cases of Prader-Willi syndrome (PWS) are associated with the physical absence of the paternal Prader-Willi chromosome region (PWCR) by deletion 15q11-13, by segmental maternal heterodisomy or by chromosome rearrangements resulting in homozygosity for maternal PWCR. In isolated/familial case