mandibulacral dysplasia and Charcot - Marie - Tooth disorder type 2B1 and mutations in LBR were reportedto causePelger - Huet anomaly
hyper- or hypo - lobulation of the nucleus ( Fig . 4often resultingin the typical pseudo - Pelger - Huet anomaly
a mutation of the lamin B receptor ( LBR ) gene located on subband 1q42.1 5(passive) is caused byPelger - Huet anomaly
a mutation in the lamin B receptor ( Hoffmann et al . , 2002(passive) caused byPelger - Huet anomaly
mutations in a nuclear lamina ( membrane ) - specifically the lamin B receptor(passive) is caused byPelger - Huet anomaly
mutations in the lamin B receptor ( LBR ) gene(passive) is caused byPelger - Huet anomaly
mutations in LBR gene(passive) is caused byPelger - Huet anomaly
abnormalities in blood cells called granulocytescausesabnormalities in blood cells called granulocytes
the number of SU(2)X doubletspreventsthe number of SU(2)X doublets
seizurescan causeseizures
the nuclei within leukocyte cells to be abnormally shaped into two distinct patterns , heterozygotes ( which make the cell appear shaped like a pair of eyeglasses or a dumbbellcausesthe nuclei within leukocyte cells to be abnormally shaped into two distinct patterns , heterozygotes ( which make the cell appear shaped like a pair of eyeglasses or a dumbbell