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MBD5 gene

Known as: FLJ11113, methyl-CpG binding domain protein 5, KIAA1461 
National Institutes of Health

Related topics

Related topics

1 relation
MBD4 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
[Genetic diagnosis of a child with aortic stenosis and thumb aplasia].
  • Dong WuQ. Hou S. Liao
  • Zhonghua yi xue yi chuan xue za zhi = Zhonghua…
  • 2018
  • Corpus ID: 51958827
OBJECTIVE To analyze the molecular mechanism and prognosis of a child with aortic stenosis and thumb aplasia. METHODS The… 
Review
2016
Review
2016
MBD5 Haploinsufficiency -- GeneReviews(®)
2015
2015
A novel interstitial deletion of 2q22.3 q23.3 in a patient with dysmorphic features, epilepsy, aganglionosis, pure red cell aplasia, and skeletal malformations
Many chromosomal deletions encompassing the 2q23.1 region have been described ranging from small deletions of 38 kb up to >19 Mb… 
2013
2013
Uncovering the molecular pathways of MBD5 in neurodevelopmental disorders
2012
2012
The Essential Role of Mbd5 in the Regulation of Somatic Growth and Glucose Homeostasis in Mice
Methyl-CpG binding domain protein 5 (MBD5) belongs to the MBD family proteins, which play central roles in transcriptional… 
2012
2012
2q23.1 microdeletion of the MBD5 gene in a female with seizures, developmental delay and distinct dysmorphic features.
2012
2012
2q23.1 microdeletion of the MBD5 gene in a female with seizures, developmental delay and distinct dysmorphic features.
2010
2010
The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype
Correction to: European Journal of Human Genetics (2010) 18, 163–170; doi:10.1038/ejhg.2009.152; published online 7 October 2009… 
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