WHSC1 wt Allele

Known as: WHS, REIIBP, TRX5 Gene 
Human WHSC1 wild-type allele is located in the vicinity of 4p16.3 and is approximately 111 kb in length. This allele, which encodes histone-lysine N… (More)

Topic mentions per year

Topic mentions per year

1985-2017
0102019852017

Papers overview

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2012
2012
Wolf-Hirschhorn syndrome (WHS) is a contiguous gene deletion disorder associated with the distal part of the short arm of… (More)
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2011
2011
Larger imbalances on chromosome 4p in the form of deletions associated with Wolf-Hirschhorn syndrome (WHS) and duplications of… (More)
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2010
2010
Wolf-Hirschhorn syndrome (WHS) is a complex congenital malformation produced by a loss of genomic material at the locus 4p16.3… (More)
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2009
2009
ilance of the primary care providers. Early diagnosis and treatment of the epilepsy almost certainly have a positive impact upon… (More)
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2007
2007
Wolf-Hirschhorn syndrome (WHS) is characterized by growth delay, developmental delay, hypotonia, seizures, feeding difficulties… (More)
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2005
2005
The Wolf-Hirschhorn syndrome (WHS), is a well known contiguous gene syndrome characterized by microcephaly, hypertelorism… (More)
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Highly Cited
2003
Highly Cited
2003
In an attempt to define the distinctive Wolf-Hirschhorn syndrome (WHS) phenotype, and to map its specific clinical manifestations… (More)
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2003
2003
BACKGROUND Wolf-Hirschhorn syndrome (WHS) is a well-known clinical entity caused by partial deletion of the short arm of one… (More)
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1999
1999
Deletions within human chromosome 4p16.3 cause Wolf-Hirschhorn syndrome (WHS), which is characterized by severe mental and… (More)
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1995
1995
We have collected and analyzed clinical information from 11 patients with chromosome 4p deletions or rearrangements characterized… (More)
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