Beckwith-Wiedemann Syndrome

Known as: beckwith syndrome, Wiedemann-Beckwith Syndromes (WBS), EMG Syndromes 
A genetic syndrome caused by abnormalities in chromosome 11. It is characterized by large birth weight, macroglossia, umbilical hernia, ear… (More)
National Institutes of Health

Papers overview

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Review
2010
Review
2010
Beckwith–Wiedemann syndrome (BWS) is a model disorder for the study of imprinting, growth dysregulation, and tumorigenesis… (More)
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Highly Cited
2009
Highly Cited
2009
Beckwith-Wiedemann syndrome (BWS) is a fetal overgrowth and human imprinting disorder resulting from the deregulation of a number… (More)
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Highly Cited
2005
Highly Cited
2005
Beckwith–Wiedemann Syndrome (BWS) results from mutations or epigenetic events involving imprinted genes at 11p15.5. Most BWS… (More)
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Highly Cited
2003
Highly Cited
2003
Beckwith-Wiedemann syndrome (BWS) is a model imprinting disorder resulting from mutations or epimutations affecting imprinted… (More)
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Highly Cited
2003
Highly Cited
2003
Recent data in humans and animals suggest that assisted reproductive technology (ART) might affect the epigenetics of early… (More)
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Highly Cited
2002
Highly Cited
2002
Beckwith-Wiedemann syndrome (BWS) presents with visceromegaly, macroglossia, tumor predisposition and other congenital… (More)
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Highly Cited
2000
Highly Cited
2000
Beckwith-Wiedemann syndrome (BWS) is a model imprinting disorder resulting from mutations or epigenetic events involving… (More)
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Highly Cited
1997
Highly Cited
1997
Mice lacking the imprinted Cdk inhibitor p57KIP2 have altered cell proliferation and differentiation, leading to abdominal muscle… (More)
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Highly Cited
1997
Highly Cited
1997
Genomic imprinting is an epigenetic chromosomal modification in the gamete or zygote causing preferential expression of a… (More)
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Highly Cited
1996
Highly Cited
1996
p57KIP2 is a potent tight-binding inhibitor of several G1 cyclin/Cdk complexes, and is a negative regulator of cell… (More)
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