期刊
EUROPEAN JOURNAL OF HUMAN GENETICS
卷 18, 期 1, 页码 8-14出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/ejhg.2009.106
关键词
Beckwith-Wiedeman syndrome; genomic imprinting; epigenetics; chromosome 11; tumor predisposition
Beckwith-Wiedemann syndrome (BWS) is a model disorder for the study of imprinting, growth dysregulation, and tumorigenesis. Unique observations in this disorder point to an important embryonic developmental window relevant to the observations of increased monozygotic twinning and an increased rate of epigenetic errors after subfertility/assisted reproduction.
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