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Journal Abstract Search

308 related items for PubMed ID: 16007606

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  • 3. [Nuclear abnormalities in Pelger-Huet anomaly; progress in blood cell morphology].
    Tomonaga M.
    Rinsho Byori; 2005 Jan; 53(1):54-60. PubMed ID: 15724491
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  • 4. 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.
    Christensen RD, Yaish HM.
    J Perinatol; 2012 Mar; 32(3):238-40. PubMed ID: 22370897
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  • 6. Pelger-Huët anomaly: a critical review of the literature.
    Speeckaert MM, Verhelst C, Koch A, Speeckaert R, Lacquet F.
    Acta Haematol; 2009 Mar; 121(4):202-6. PubMed ID: 19468205
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  • 7. Historical perspective and clinical implications of the Pelger-Hüet cell.
    Cunningham JM, Patnaik MM, Hammerschmidt DE, Vercellotti GM.
    Am J Hematol; 2009 Feb; 84(2):116-9. PubMed ID: 19021122
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  • 8. Lamin B-receptor mutations in Pelger-Huët anomaly.
    Best S, Salvati F, Kallo J, Garner C, Height S, Thein SL, Rees DC.
    Br J Haematol; 2003 Nov; 123(3):542-4. PubMed ID: 14617022
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  • 9. Pelger-Huet anomaly: a case report.
    Anand M, Kumar R, Raina V.
    Indian J Pathol Microbiol; 2007 Jul; 50(3):661-2. PubMed ID: 17883176
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  • 10. [The Pelger-Huët leukocyte nuclear anomaly: a morphologic, cytochemical, cytogenetic and ultrastructural study of 39 cases (authors' transl)].
    Milanesi B.
    Quad Sclavo Diagn; 1980 Dec; 15(4):1097-115. PubMed ID: 7454963
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  • 11. [Pelger-Huët anomaly and hereditary elliptocytosis in 2 siblings].
    Urbina-Guerrero JR, Muñoz-Quiles I, Linaldi-Camacho A.
    Bol Med Hosp Infant Mex; 1992 Jul; 49(7):454-8. PubMed ID: 1418654
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  • 12. Tuberculosis and Pelger-Huët anomaly. Case report.
    Cicchitto G, Parravicini M, De Lorenzo S, Di Pisa G, Malacrida A.
    Panminerva Med; 1999 Dec; 41(4):367-9. PubMed ID: 10705722
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  • 13. Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomaly.
    Shultz LD, Lyons BL, Burzenski LM, Gott B, Samuels R, Schweitzer PA, Dreger C, Herrmann H, Kalscheuer V, Olins AL, Olins DE, Sperling K, Hoffmann K.
    Hum Mol Genet; 2003 Jan 01; 12(1):61-9. PubMed ID: 12490533
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  • 14. [The Pelger-Huet granulocytic anomaly: first report of 2 homozygous subjects in the same family].
    Riario-Sforza G, Salvati F, Troya C.
    Arch Sci Med (Torino); 1981 Jan 01; 138(4):511-5. PubMed ID: 7340736
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  • 15. [Pelger-Huet anomaly].
    Malcić I, Tiefenbach A.
    Bilt Hematol Transfuz; 1979 Jan 01; 7(1 Suppl):3-7. PubMed ID: 553508
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  • 16. [A case of Pelger-Huet anomaly in a premature infant].
    Kallo J, Malina A, Malinová V, Pennigerová S.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1989 Jan 01; 116(1):145-9. PubMed ID: 2472317
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  • 17. Pelger-huet anomaly and a mild skeletal phenotype secondary to mutations in LBR.
    Borovik L, Modaff P, Waterham HR, Krentz AD, Pauli RM.
    Am J Med Genet A; 2013 Aug 01; 161A(8):2066-73. PubMed ID: 23824842
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  • 18. Pseudo-Pelger-Huët in kidney-transplanted patients.
    Dusse LM, Morais E Silva RM, Freitas VM, Medeiros de Paula GM, Vieira LM, Carvalho Md.
    Acta Haematol; 2006 Aug 01; 116(4):272-4. PubMed ID: 17119329
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  • 19. Deletion of LBR N-terminal domains recapitulates Pelger-Huet anomaly phenotypes in mouse without disrupting X chromosome inactivation.
    Young AN, Perlas E, Ruiz-Blanes N, Hierholzer A, Pomella N, Martin-Martin B, Liverziani A, Jachowicz JW, Giannakouros T, Cerase A.
    Commun Biol; 2021 Apr 12; 4(1):478. PubMed ID: 33846535
    [Abstract] [Full Text] [Related]

  • 20. [Pelger-Huët anomaly. Cases in a Mexican family].
    Muñoz-Quiles I, Saldaña-García EA.
    Bol Med Hosp Infant Mex; 1987 Jan 12; 44(1):21-5. PubMed ID: 3814331
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