RNASE12 gene

Known as: RAI1, RNASE12, ribonuclease A family member 12 (inactive) 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2000-2017
024620002017

Papers overview

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2010
2010
Smith-Magenis syndrome (SMS; OMIM 182290) is a neurodevelopmental disorder characterized by a well-defined pattern of anomalies… (More)
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2009
2009
Disorders with overlapping diagnostic features are grouped into a network module. Based on phenotypic similarities or… (More)
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Highly Cited
2006
Highly Cited
2006
Purpose: Smith-Magenis syndrome (SMS) is a complex disorder that includes mental retardation, craniofacial and skeletal anomalies… (More)
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2006
2006
Genomic disorders are conditions that result from DNA rearrangements, such as deletions or duplications. The identification of… (More)
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2006
2006
BACKGROUND Our previous studies have shown a significant linkage of intracranial aneurysms (IAs) to chromosome 17. METHODS AND… (More)
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2005
2005
Retinoic acid induced 1 (RAI1) is among the 20 genes identified in the critical region of Smith-Magenis syndrome (SMS), a genomic… (More)
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2004
2004
Smith-Magenis syndrome (SMS) is a multiple congenital anomaly/mental retardation syndrome associated with del(17)(p11.2p11.2… (More)
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2001
2001
The human chromosomal band 17p11.2 is a genetically unstable interval. It has been shown to be deleted in patients suffering from… (More)
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2000
2000
The RAT1 gene of Saccharomyces cerevisiae encodes a 5'-->3' exoribonuclease which plays an essential role in yeast RNA… (More)
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2000
2000
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant disorder caused by the expansion of a polymorphic (CAG)(n) tract… (More)
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