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    Results: 1 to 20 of 278

    1.

    Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypes.

    Oosterwijk JC, Mansour S, van Noort G, Waterham HR, Hall CM, Hennekam RC.

    J Med Genet. 2003 Dec;40(12):937-41. Review. No abstract available. PMID: 14684694 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Benign anomaly to malign dysplasia: variable expression of lamin B receptor mutations in humans.

    Kasbekar DP.

    J Biosci. 2004 Dec;29(4):367-8. No abstract available. PMID: 15625388 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    HEM dysplasia and ichthyosis are likely laminopathies and not due to 3beta-hydroxysterol Delta14-reductase deficiency.

    Wassif CA, Brownson KE, Sterner AL, Forlino A, Zerfas PM, Wilson WK, Starost MF, Porter FD.

    Hum Mol Genet. 2007 May 15;16(10):1176-87. Epub 2007 Apr 2.PMID: 17403717 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Greenberg dysplasia (HEM) and lethal X linked dominant Conradi-Hünermann chondrodysplasia punctata (CDPX2): presentation of two cases with overlapping phenotype.

    Offiah AC, Mansour S, Jeffrey I, Nash R, Whittock N, Pyper R, Bewley S, Clayton PT, Hall CM.

    J Med Genet. 2003 Dec;40(12):e129. No abstract available. PMID: 14684697 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Greenberg dysplasia (hydrops-ectopic calcification-moth-eaten skeletal dysplasia): prenatal ultrasound diagnosis and review of literature.

    Trajkovski Z, Vrcakovski M, Saveski J, Gucev ZS.

    Am J Med Genet. 2002 Sep 1;111(4):415-9.PMID: 12210303 [PubMed - indexed for MEDLINE]Related articles

    6.

    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 1;12(1):61-9.PMID: 12490533 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    [Pelger-Huet anomaly observed in a Warsaw family]

    Wrõblewska-Cieliszak K.

    Pediatr Pol. 1971 Sep;46(9):1157-61. Polish. No abstract available. PMID: 5122481 [PubMed - indexed for MEDLINE]Related articles

    8.

    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.PMID: 10705722 [PubMed - indexed for MEDLINE]Related articles

    9.

    [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;116(1):145-9. German. PMID: 2472317 [PubMed - indexed for MEDLINE]Related articles

    10.

    [Acute leukemia secondary to idiopathic myelofibrosis with homozygote pseudo-Pelger anomaly and complex chromosomal changes]

    Tosato F, Fossaluzza V, Bortotto L, Bartolomei P.

    Minerva Med. 1986 May 31;77(22-23):1023-6. Italian. PMID: 3459966 [PubMed - indexed for MEDLINE]Related articles

    11.

    [Case of Pelger-Huet anomaly in its exceptional homozygotic variant]

    Ciatto A, Ferretti GF.

    Minerva Med. 1978 Mar 3;69(11):697-700. Italian. PMID: 643213 [PubMed - indexed for MEDLINE]Related articles

    12.

    Hydrops-ectopic calcification-moth-eaten skeletal dysplasia (Greenberg dysplasia): prenatal diagnosis and further delineation of a rare genetic disorder.

    Chitayat D, Gruber H, Mullen BJ, Pauzner D, Costa T, Lachman R, Rimoin DL.

    Am J Med Genet. 1993 Aug 15;47(2):272-7. Review.PMID: 8213919 [PubMed - indexed for MEDLINE]Related articles

    13.

    [Constitutional familial leucocytopenia with partial Pelger anomaly and delayed development of bone (author's transl)]

    Heyne K.

    Eur J Pediatr. 1976 Feb 4;121(3):191-201. German. PMID: 1248491 [PubMed - indexed for MEDLINE]Related articles

    14.

    [Nuclear abnormalities in Pelger-Huet anomaly; progress in blood cell morphology]

    Tomonaga M.

    Rinsho Byori. 2005 Jan;53(1):54-60. Review. Japanese. PMID: 15724491 [PubMed - indexed for MEDLINE]Related articles

    15.

    Pelger-Huet anomaly in an infant with multiple congenital anomalies.

    Fishbein JD, Falletta JM.

    Am J Hematol. 1991 Nov;38(3):240-2.PMID: 1951327 [PubMed - indexed for MEDLINE]Related articles

    16.

    Homozygous form of the Pelger-Huët leukocyte anomaly in man.

    Aznar J, Vaya A.

    Acta Haematol. 1981;66(1):59-62.PMID: 6794302 [PubMed - indexed for MEDLINE]Related articles

    17.

    The acrofacial dysostoses--a wide spectrum of overlapping phenotypes.

    Dimitrov B, Balikova I, Bradinova I, Zahariev D, Popova A, Simeonov E, De Smet L, Devriendt K, Fryns JP.

    Genet Couns. 2005;16(2):181-6. No abstract available. PMID: 16080300 [PubMed - indexed for MEDLINE]Related articles

    18.

    Detailed ultrasonographic findings in Greenberg dysplasia.

    Madazli R, Aksoy F, Ocak V, Atasü T.

    Prenat Diagn. 2001 Jan;21(1):65-7.PMID: 11180245 [PubMed - indexed for MEDLINE]Related articles

    19.

    Congenital Pelger-Huet anomaly in triplets.

    Ware R, Kurtzberg J, Brazy J, Falletta JM.

    Am J Hematol. 1988 Mar;27(3):226-7.PMID: 3348208 [PubMed - indexed for MEDLINE]Related articles

    20.

    [Familial Pelger-Huet anomaly simulating pathological "left-shift" in the blood picture]

    Augustyniak W, Hilt J, Romanowska-Górecka B.

    Wiad Lek. 1979 Nov 15;32(22):1643-5. Polish. No abstract available. PMID: 538918 [PubMed - indexed for MEDLINE]Related articles

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