Co-Authors
                            
                            
                                This is a "connection" page, showing publications co-authored by   PILAR MAGOULAS   and   LORRAINE POTOCKI.
                            
                            
                            
                                
                                    
                                            
    
        
        
        
            Connection Strength
            
                
            
            0.654
         
        
        
     
 
    
        
        - 
            Inherited dup(17)(p11.2p11.2): expanding the phenotype of the Potocki-Lupski syndrome. Am J Med Genet A. 2014 Feb; 164A(2):500-4.
            
            
                Score: 0.438
            
         
        
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            Syndromic congenital myelofibrosis associated with a loss-of-function variant in RBSN. Blood. 2018 08 09; 132(6):658-662.
            
            
                Score: 0.149
            
         
        
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            Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management. JAMA Pediatr. 2017 12 04; 171(12):e173438.
            
            
                Score: 0.036
            
         
        
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            Nonrecurrent 17p11.2p12 Rearrangement Events that Result in Two Concomitant Genomic Disorders: The PMP22-RAI1 Contiguous Gene Duplication Syndrome. Am J Hum Genet. 2015 Nov 05; 97(5):691-707.
            
            
                Score: 0.031