| Beckwith-Wiedemann syndrome. | |
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MedLine Citation:
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PMID: 19550435 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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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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Authors:
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Rosanna Weksberg; Cheryl Shuman; J Bruce Beckwith |
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Publication Detail:
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Type: Journal Article; Review |
Journal Detail:
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Title: European journal of human genetics : EJHG Volume: 18 ISSN: 1476-5438 ISO Abbreviation: Eur. J. Hum. Genet. Publication Date: 2010 Jan |
Date Detail:
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Created Date: 2009-12-16 Completed Date: 2010-02-22 Revised Date: 2011-07-19 |
Medline Journal Info:
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Nlm Unique ID: 9302235 Medline TA: Eur J Hum Genet Country: England |
Other Details:
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Languages: eng Pagination: 8-14 Citation Subset: IM |
Affiliation:
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Department of Genetics and Genome Biology, The Hospital for Sick Children, 555 University Ave., Toronto, Ontario M5G 1X8, Canada. rweksb@sickkids.ca |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Beckwith-Wiedemann Syndrome
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diagnosis,
genetics*,
therapy Diagnosis, Differential Genetic Counseling Genetic Testing Humans |
| Comments/Corrections | |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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