Is gestation in Prader-Willi syndrome affected by the genetic subtype?

BACKGROUND: Prader-Willi syndrome (PWS) is a complex genetic disorder with errors in genomic imprinting, generally due to a paternal deletion of chromosome 15q11-q13 region. Maternal disomy 15 (both 15s from the mother) is the second most common form of PWS resulting from a trisomic zygote followed...

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Bibliographic Details
Main Authors: Butler, Merlin G., Sturich, Jennifer, Myers, Susan E., Gold, June-Anne, Kimonis, Virginia, Driscoll, Daniel J.
Format: Artigo
Language:Inglês
Published: Springer US 2009
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Short Communication
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC2767487/
https://ncbi.nlm.nih.gov/pubmed/19760168
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10815-009-9341-7
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