Pelger–Huët anomaly in a child with 1q42.3-44 deletion
Author:
Publisher
Wiley
Subject
Oncology,Hematology,Pediatrics, Perinatology and Child Health
Reference20 articles.
1. Blood. Textbook of hematology. Boston: Little, Brown; 1996. 788–789 pp.
2. . Hematology of infancy and childhood. Philadelphia: W.B. Saunders; 1998. 1870 p.
3. The Pelger Anomaly of Leukocytes: Forty-One Cases in Seven Families
4. Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger–Huët anomaly)
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1. Morphology of blood cells;Blood Cells;2021-12-31
2. A neonate with the Pelger–Huët anomaly, cleft lip and palate, and agenesis of the corpus callosum, with a chromosomal microdeletion involving 1q41 to 1q42.12;Journal of Perinatology;2012-02-28
3. New cases and refinement of the critical region in the 1q41q42 microdeletion syndrome;European Journal of Medical Genetics;2011-01
4. Lamin B receptor;Nucleus;2010-01
5. Granulocytic Disorders;Hematopathology;2008
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