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    Results: 20

    1.

    Implication of long-distance regulation of the HOXA cluster in a patient with postaxial polydactyly.

    Lodder EM, Eussen BH, van Hassel DA, Hoogeboom AJ, Poddighe PJ, Coert JH, Oostra BA, de Klein A, de Graaff E.

    Chromosome Res. 2009;17(6):737-44. Epub 2009 Aug 12.PMID: 19672683 [PubMed - in process]Related articlesFree article

    2.

    Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions.

    Guelen L, Pagie L, Brasset E, Meuleman W, Faza MB, Talhout W, Eussen BH, de Klein A, Wessels L, de Laat W, van Steensel B.

    Nature. 2008 Jun 12;453(7197):948-51. Epub 2008 May 7.PMID: 18463634 [PubMed - indexed for MEDLINE]Related articles

    3.

    A familial inverted duplication 2q33-q34 identified and delineated by multiple cytogenetic techniques.

    Eussen BH, van de Laar I, Douben H, van Kempen L, Hochstenbach R, De Man SA, Van Opstal D, de Klein A, Poddighe PJ.

    Eur J Med Genet. 2007 Mar-Apr;50(2):112-9. Epub 2006 Nov 3.PMID: 17161033 [PubMed - indexed for MEDLINE]Related articles

    4.

    Large deletion at the TSC1 locus in a family with tuberous sclerosis complex.

    Nellist M, Sancak O, Goedbloed MA, van Veghel-Plandsoen M, Maat-Kievit A, Lindhout D, Eussen BH, de Klein A, Halley DJ, van den Ouweland AM.

    Genet Test. 2005 Fall;9(3):226-30.PMID: 16225402 [PubMed - indexed for MEDLINE]Related articles

    5.

    Isolated postaxial polydactyly type B with mosaicism of a submicroscopic unbalanced translocation leading to an extended phenotype in offspring.

    Galjaard RJ, van der Linde HC, Eussen BH, de Vries BB, Wouters CH, Oostra BA, de Graaff E, Heutink P.

    Am J Med Genet A. 2003 Aug 30;121A(2):168-73.PMID: 12910499 [PubMed - indexed for MEDLINE]Related articles

    6.

    CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder.

    Verkerk AJ, Mathews CA, Joosse M, Eussen BH, Heutink P, Oostra BA; Tourette Syndrome Association International Consortium for Genetics.

    Genomics. 2003 Jul;82(1):1-9.PMID: 12809671 [PubMed - indexed for MEDLINE]Related articles

    7.

    Large deletion causing the TSC2-PKD1 contiguous gene syndrome without infantile polycystic disease.

    Smulders YM, Eussen BH, Verhoef S, Wouters CH.

    J Med Genet. 2003 Feb;40(2):E17. No abstract available. PMID: 12566535 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization.

    Veltman JA, Schoenmakers EF, Eussen BH, Janssen I, Merkx G, van Cleef B, van Ravenswaaij CM, Brunner HG, Smeets D, van Kessel AG.

    Am J Hum Genet. 2002 May;70(5):1269-76. Epub 2002 Apr 9.PMID: 11951177 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Quantification of MYCN, DDX1, and NAG gene copy number in neuroblastoma using a real-time quantitative PCR assay.

    De Preter K, Speleman F, Combaret V, Lunec J, Laureys G, Eussen BH, Francotte N, Board J, Pearson AD, De Paepe A, Van Roy N, Vandesompele J.

    Mod Pathol. 2002 Feb;15(2):159-66.PMID: 11850545 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    A novel gene on human chromosome 2p24 is differentially expressed between androgen-dependent and androgen-independent prostate cancer cells.

    Chang GT, Steenbeek M, Schippers E, Blok LJ, van Weerden WM, van Alewijk DC, Eussen BH, van Steenbrugge GJ, Brinkmann AO.

    Eur J Cancer. 2001 Nov;37(16):2129-34.PMID: 11597395 [PubMed - indexed for MEDLINE]Related articles

    11.

    Characterization of a zinc-finger protein and its association with apoptosis in prostate cancer cells.

    Chang GT, Steenbeek M, Schippers E, Blok LJ, van Weerden WM, van Alewijk DC, Eussen BH, van Steenbrugge GJ, Brinkmann AO.

    J Natl Cancer Inst. 2000 Sep 6;92(17):1414-21.PMID: 10974077 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.

    Warburton PE, Dolled M, Mahmood R, Alonso A, Li S, Naritomi K, Tohma T, Nagai T, Hasegawa T, Ohashi H, Govaerts LC, Eussen BH, Van Hemel JO, Lozzio C, Schwartz S, Dowhanick-Morrissette JJ, Spinner NB, Rivera H, Crolla JA, Yu C, Warburton D.

    Am J Hum Genet. 2000 Jun;66(6):1794-806. Epub 2000 Apr 24. Review.PMID: 10777715 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito.

    Eussen BH, Bartalini G, Bakker L, Balestri P, Di Lucca C, Van Hemel JO, Dauwerse H, van Den Ouweland AM, Ris-Stalpers C, Verhoef S, Halley DJ, Fois A.

    J Med Genet. 2000 Apr;37(4):287-91.PMID: 10745047 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14).

    de Vries BB, Eussen BH, van Diggelen OP, van Der Heide A, Deelen WH, Govaerts LC, Lindhout D, Wouters CH, Van Hemel JO.

    Am J Med Genet. 1999 Nov 19;87(2):189-94.PMID: 10533035 [PubMed - indexed for MEDLINE]Related articles

    15.

    Identification of a gene on human chromosome 8q11 that is differentially expressed during prostate-cancer progression.

    Chang GT, Tapsi N, Steenbeek M, Blok LJ, van Weerden WM, van Alewijk DC, Eussen BH, van Steenbrugge GJ, Brinkmann AO.

    Int J Cancer. 1999 Nov 12;83(4):506-11.PMID: 10508487 [PubMed - indexed for MEDLINE]Related articles

    16.

    Expression of differentiation-related genes in colorectal cancer: possible implications for prognosis.

    van Belzen N, Dinjens WN, Eussen BH, Bosman FT.

    Histol Histopathol. 1998 Oct;13(4):1233-42. Review.PMID: 9810514 [PubMed - indexed for MEDLINE]Related articles

    17.

    The murine CYLN2 gene: genomic organization, chromosome localization, and comparison to the human gene that is located within the 7q11.23 Williams syndrome critical region.

    Hoogenraad CC, Eussen BH, Langeveld A, van Haperen R, Winterberg S, Wouters CH, Grosveld F, De Zeeuw CI, Galjart N.

    Genomics. 1998 Nov 1;53(3):348-58.PMID: 9799601 [PubMed - indexed for MEDLINE]Related articles

    18.

    A chromosome 21-specific cosmid cocktail for the detection of chromosome 21 aberrations in interphase nuclei.

    van Opstal D, van Hemel JO, Eussen BH, van der Heide A, van den Berg C, In 'T Veld PA, Los FJ.

    Prenat Diagn. 1995 Aug;15(8):705-11.PMID: 7479588 [PubMed - indexed for MEDLINE]Related articles

    19.

    Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data.

    Hamel BC, Smits AP, de Graaff E, Smeets DF, Schoute F, Eussen BH, Knight SJ, Davies KE, Assman-Hulsmans CF, Oostra BA.

    Am J Hum Genet. 1994 Nov;55(5):923-31.PMID: 7977354 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Limited size of the fragile X site shown by fluorescence in situ hybridization.

    Verkerk AJ, Eussen BH, Van Hemel JO, Oostra BA.

    Am J Med Genet. 1992 Apr 15-May 1;43(1-2):187-91.PMID: 1605191 [PubMed - indexed for MEDLINE]Related articles

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