Understanding and recognizing the Pelger-Huët anomaly

American Journal of Clinical Pathology

Volumn 137, Issue 3, 2012, Pages 358-366

  Colella, Rita ^a   Hollensead, Sandra C ^a  

^a University of Louisville School of Medicine   (United States)

Author keywords

Lamin B receptor; Lamins; Leukemoid reaction; Myelodysplasia; Pelger Hu t anomaly; Polymorphonuclear leukocyte; Pseudo Pelger Hu t anomaly

Indexed keywords

LAMIN B RECEPTOR; RECEPTOR PROTEIN; UNCLASSIFIED DRUG; CELL RECEPTOR; LAMIN;

BLOOD SMEAR; DISEASE CLASSIFICATION; DOCTOR PATIENT RELATION; GENE MUTATION; GRANULOCYTE; HEMATOLOGIC DISEASE; HUMAN; LABORATORY TEST; LEUKOCYTE DISORDER; MOLECULAR RECOGNITION; MORPHOLOGY; NEUTROPHIL; PRIORITY JOURNAL; REVIEW; CELL NUCLEUS; DIFFERENTIAL DIAGNOSIS; FAMILY HEALTH; GENETICS; LEUKEMOID REACTION; METABOLISM; MUTATION; MYELODYSPLASTIC SYNDROME; PATHOLOGY;

CELL NUCLEUS; DIAGNOSIS, DIFFERENTIAL; FAMILY HEALTH; HUMANS; LAMINS; LEUKEMOID REACTION; MUTATION; MYELODYSPLASTIC SYNDROMES; NEUTROPHILS; PELGER-HUET ANOMALY; RECEPTORS, CYTOPLASMIC AND NUCLEAR;

EID: 84859262785     PISSN: 00029173     EISSN: 19437722     Source Type: Journal    
DOI: 10.1309/AJCP3G8MDUXYSCID     Document Type: Review

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