CHRISTINE  ENG  to  Micrognathism
                            
                            
                                This is a "connection" page, showing publications  CHRISTINE  ENG  has written about  Micrognathism.
                            
                            
                            
                                
                                    
                                            
    
        
        
        
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            0.332
         
        
        
     
 
    
        
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            Retrospective analysis of a clinical exome sequencing cohort reveals the mutational spectrum and identifies candidate disease-associated loci for BAFopathies. Genet Med. 2022 02; 24(2):364-373.
            
            
                Score: 0.180
             
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            De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. Am J Hum Genet. 2015 Dec 03; 97(6):904-13.
            
            
                Score: 0.119
             
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            Heterozygous variants in ACTL6A, encoding a component of the BAF complex, are associated with intellectual disability. Hum Mutat. 2017 10; 38(10):1365-1371.
            
            
                Score: 0.033