ZNF236 gene

Known as: ZINC FINGER PROTEIN 236, ZNF236, ZNF236A 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1999-2016
01219992016

Papers overview

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2017
2017
BACKGROUND Childhood disintegrative disorder (CDD) is a rare form of autism spectrum disorder (ASD) of unknown etiology. It is… (More)
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2016
Review
2016
Deletions of the long arm of chromosome 18 cause a common autosomal syndrome clinically characterized by a protean clinical… (More)
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2011
2011
Nonsyndromic cleft palate (CP) is a common birth defect with a complex and heterogeneous etiology involving both genetic and… (More)
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Review
2006
Review
2006
OBJECTIVE 18q deletion syndrome is a multiple-anomaly mental retardation syndrome associated with congenital aural atresia. The… (More)
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2003
2003
Diabetic nephropathy (DN) is the most common cause of renal failure in the western hemisphere. Epidemiological studies have… (More)
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2003
2003
We report on a 12-year-old boy who presented with delayed development and CNS dysmyelination. Genetic studies showed a normal 46… (More)
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1999
1999
We report the cDNA cloning and characterization of ZNF236, a novel Kruppel-like zinc-finger gene initially identified by its… (More)
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