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Identification of Novel Imprinted Transcripts in the Prader-Willi Syndrome and Angelman Syndrome Deletion Region: Further Evidence for Regional Imprinting Control

Deletions and other abnormalities of human chromosome 15q11-q13 are associated with two developmental disorders, Prader-Willi syndrome (PWS) and Angelman syndrome (AS). Loss of expression of imprinted, paternally expressed genes has been implicated in PWS. However, the number of imprinted genes that...

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Bibliografske podrobnosti
Main Authors: Lee, Syann, Wevrick, Rachel
Format: Artigo
Jezik:Inglês
Izdano: The American Society of Human Genetics 2000
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1288168/
https://ncbi.nlm.nih.gov/pubmed/10712201
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