Literature DB >> 10457411

Homozygous form of the Pelger-Huët anomaly.

J G Erice1, J M Pérez, F S Pericás.   

Abstract

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Year:  1999        PMID： 10457411

Source DB:  PubMed          Journal:  Haematologica        ISSN： 0390-6078            Impact factor:   9.941


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  3 in total

1.  An anadysplasia-like, spontaneously remitting spondylometaphyseal dysplasia secondary to lamin B receptor (LBR) gene mutations: further definition of the phenotypic heterogeneity of LBR-bone dysplasias.

Authors:  Nara Sobreira; Peggy Modaff; Gary Steel; Jing You; Sonia Nanda; Julie Hoover-Fong; David Valle; Richard M Pauli
Journal:  Am J Med Genet A       Date:  2014-10-27       Impact factor: 2.802

2.  Case of acquired or pseudo-Pelger-Huët anomaly.

Authors:  Mohamed S Ayan; Abd Almonem M Abdelrahman; Nabin Khanal; Osama S Elsallabi; Nathan C Birch
Journal:  Oxf Med Case Reports       Date:  2015-04-01

3.  Mouse neutrophils lacking lamin B-receptor expression exhibit aberrant development and lack critical functional responses.

Authors:  Peter Gaines; Chiung W Tien; Ada L Olins; Donald E Olins; Leonard D Shultz; Lisa Carney; Nancy Berliner
Journal:  Exp Hematol       Date:  2008-06-11       Impact factor: 3.084
  3 in total

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