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    Predicted Benign and Synonymous variants in CYP11A1 Causes Primary Adrenal Insufficiency through Missplicing
 
      
  
    Copy number variation: a prognostic marker for young patients with squamous cell carcinoma of the oral tongue
 
      
  
    Copy number variation: a prognostic marker for young patients with squamous cell carcinoma of the oral tongue
 
      
  
    Detecting Genetics Modifiers of Spondyloepimetaphyseal Dysplasia with Joint Laxity (SEMDJL) in the Caucasian Afrikaner community
 
      
  
    Novel variants in natriuretic peptide receptor 2 in unrelated patients with acromesomelic dysplasia type Maroteaux
 
      
  
    The gut microbiome of Mexican children affected by obesity
 
      
  
    Human serum albumin alters specific genes that can play a role in survival and persistence in Acinetobacter baumannii
 
      
  
    Novel mutations in ALDH1A3 associated with autosomal recessive anophthalmia/microphthalmia, and review of the literature
 
      
  
    A splice site variant in INPP5E causes diffuse cystic renal dysplasia and hepatic fibrosis in dogs
 
      
  
    Organism-environment interactions and differential gene expression patterns among open-coastal and estuarine populations of Porphyra umbilicalis Kützing (Rhodophyta) in the Northwest Atlantic
