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Article

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

Journal of assisted reproduction and genetics - 1 Aug 2009

Butler Merlin G, Sturich Jennifer, Myers Susan E, Gold June-Anne, Kimonis Virginia, Driscoll Daniel J

Abstract excerpt

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 by trisomy rescue in early pregnancy and loss of the paternal chromosome 15. However, trisomy 15 or mosaicism for...

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Source

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Identifiers

PMID: 19760168
DOI: 10.1007/s10815-009-9341-7
PMCID: PMC2767487

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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