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15q24 Microdeletion

Known as: 15q24 Deletion, 15q24 Microdeletion Syndrome, Interstitial Deletion of Chromosome 15q24 
National Institutes of Health

Papers overview

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2019
2019
OBJECTIVE To explore the genetic basis for three patients with development delay and to correlate their clinical phenotypes with… 
2017
2017
BACKGROUND Chromosome 15q24 microdeletion syndrome is a rare disease. To date, only 40 cases have been reported. Here, we also… 
2017
2017
OBJECTIVE To assess the value of chromosome microarray analysis (CMA) for identifying the etiology of developmental delay… 
Review
2016
Review
2016
In January 2012, a review of the cases of chromosome 15q24 microdeletion syndrome was published. However, this study did not… 
2013
2013
Deafness-dystonia-optic neuronopathy (DDON), or Mohr-Tranebjaerg syndrome (MTS) (Mendelian Inheritance in Man [MIM] no. 304700… 
2010
2010
Correction to: European Journal of Human Genetics advance online publication 7 October 2009; doi: 10.1038/ejhg.2009.152 Since the…