congenital pelger anomaly

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Congenital Pelger–Huët anomaly. Royalty Free Stock Photo
Congenital Pelger–Huët anomaly. Royalty Free Stock Photo
   
   
   
   
   
Congenital Pelger–Huët anomaly.
   
   
   
   
   
   
   
Congenital Pelger–Huët anomaly. It is a blood laminopathy associated with the lamin B receptor, wherein several types of white blood cells (neutrophils and eosinophils) have nuclei with unusual shape. Wright x1000.


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