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ZNF41 gene

Known as: MGC8941, MRX89, ZINC FINGER PROTEIN 41 
 
National Institutes of Health

Papers overview

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2014
2014
Objective To validate zinc finger protein 41( ZNF41) as a serum candidate biomarker in patients with ventricular septal defect… Expand
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2013
2013
We present a new idiopathic intellectual disability syndrome accompanied with distinctive facial dysmorphology. X-chromosome… Expand
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2012
2012
About 10% of causative mutations for mental retardation in male patients involve X chromosome (X-linked mental retardation, XLMR… Expand
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2010
2010
ZNF630 is a member of the primate-specific Xp11 zinc finger gene cluster that consists of six closely related genes, of which… Expand
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Review
2005
Review
2005
Mental retardation is more common in males than females in the population, assumed to be due to mutations on the X chromosome… Expand
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Highly Cited
2003
Highly Cited
2003
Nonsyndromic X-linked mental retardation (MRX) is defined by an X-linked inheritance pattern of low IQ, problems with adaptive… Expand
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1999
1999
ZNF41 belongs to a cluster of human zinc finger genes residing within a gene-rich region at Xp11.23. ZNF41 encodes a KRAB/FPB (Kr… Expand
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1991
1991
We have isolated a novel human zinc finger gene, ZNF41, from a human X-chromosome-specific library. Nucleotide sequence analysis… Expand
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