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    Results: 1 to 20 of 205

    1.

    Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.

    Barber JC, Joyce CA, Collinson MN, Nicholson JC, Willatt LR, Dyson HM, Bateman MS, Green AJ, Yates JR, Dennis NR.

    J Med Genet. 1998 Jun;35(6):491-6.PMID: 9643291 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Duplication of chromosome region 8p23.1-->p23.3: a benign variant?

    Engelen JJ, Moog U, Evers JL, Dassen H, Albrechts JC, Hamers AJ.

    Am J Med Genet. 2000 Mar 6;91(1):18-21.PMID: 10751083 [PubMed - indexed for MEDLINE]Related articles

    3.

    Duplication of 8p23.2: a benign cytogenetic variant?

    Harada N, Takano J, Kondoh T, Ohashi H, Hasegawa T, Sugawara H, Ida T, Yoshiura K, Ohta T, Kishino T, Kajii T, Niikawa N, Matsumoto N.

    Am J Med Genet. 2002 Aug 15;111(3):285-8.PMID: 12210324 [PubMed - indexed for MEDLINE]Related articles

    4.

    8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.

    Barber JC, Maloney VK, Huang S, Bunyan DJ, Cresswell L, Kinning E, Benson A, Cheetham T, Wyllie J, Lynch SA, Zwolinski S, Prescott L, Crow Y, Morgan R, Hobson E.

    Eur J Hum Genet. 2008 Jan;16(1):18-27. Epub 2007 Oct 17.PMID: 17940555 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level.

    Barber JC, Maloney V, Hollox EJ, Stuke-Sontheimer A, du Bois G, Daumiller E, Klein-Vogler U, Dufke A, Armour JA, Liehr T.

    Eur J Hum Genet. 2005 Oct;13(10):1131-6.PMID: 16077733 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Novel deletion variants of 9q13-q21.12 and classical euchromatic variants of 9q12/qh involve deletion, duplication and triplication of large tracts of segmentally duplicated pericentromeric euchromatin.

    Willatt LR, Barber JC, Clarkson A, Simonic I, Raymond FL, Docherty Z, Ogilvie CM.

    Eur J Hum Genet. 2007 Jan;15(1):45-52. Epub 2006 Sep 20.PMID: 16985501 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Duplication of 9 p11.2-p13.1: a benign cytogenetic variant.

    Di Giacomo MC, Cesarano C, Bukvic N, Manisali E, Guanti G, Susca F.

    Prenat Diagn. 2004 Aug;24(8):619-22.PMID: 15305349 [PubMed - indexed for MEDLINE]Related articles

    8.

    Direct duplication of 8p21.3-->p23.1: a cytogenetic anomaly associated with developmental delay without consistent clinical features.

    Fan YS, Siu VM, Jung JH, Farrell SA, Côté GB.

    Am J Med Genet. 2001 Oct 15;103(3):231-4.PMID: 11745996 [PubMed - indexed for MEDLINE]Related articles

    9.

    Transmitted duplication of 8p23.1-8p23.2 associated with speech delay, autism and learning difficulties.

    Glancy M, Barnicoat A, Vijeratnam R, de Souza S, Gilmore J, Huang S, Maloney VK, Thomas NS, Bunyan DJ, Jackson A, Barber JC.

    Eur J Hum Genet. 2009 Jan;17(1):37-43. Epub 2008 Aug 20.PMID: 18716609 [PubMed - indexed for MEDLINE]Related articles

    10.

    A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones.

    Popp S, Jauch A, Schindler D, Speicher MR, Lengauer C, Donis-Keller H, Riethman HC, Cremer T.

    Hum Genet. 1993 Dec;92(6):527-32.PMID: 8262510 [PubMed - indexed for MEDLINE]Related articles

    11.

    Delimitation of duplicated segments and identification of their parental origin in two partial chromosome 3p duplications.

    Antonini S, Kim CA, Sugayama SM, Vianna-Morgante AM.

    Am J Med Genet. 2002 Nov 22;113(2):144-50.PMID: 12407704 [PubMed - indexed for MEDLINE]Related articles

    12.

    Unmasking Kabuki syndrome: chromosome 8p22-8p23.1 duplication revealed by comparative genomic hybridization and BAC-FISH.

    Milunsky JM, Huang XL.

    Clin Genet. 2003 Dec;64(6):509-16.PMID: 14986831 [PubMed - indexed for MEDLINE]Related articles

    13.

    Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2.

    Giorda R, Ciccone R, Gimelli G, Pramparo T, Beri S, Bonaglia MC, Giglio S, Genuardi M, Argente J, Rocchi M, Zuffardi O.

    Hum Mutat. 2007 May;28(5):459-68.PMID: 17262805 [PubMed - indexed for MEDLINE]Related articles

    14.

    Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.

    Wyandt HE, Shim SH, Mark HF, Huang XL, Milunsky JM.

    Exp Mol Pathol. 2006 Jun;80(3):262-6. Epub 2006 Mar 6.PMID: 16516886 [PubMed - indexed for MEDLINE]Related articles

    15.

    The application of region-specific probes for the resolution of duplication 8p: a case report and a review of the literature.

    Pabst B, Arslan-Kirchner M, Schmidtke J, Miller K.

    Cytogenet Genome Res. 2003;103(1-2):3-7. Review.PMID: 15004455 [PubMed - indexed for MEDLINE]Related articles

    16.

    Loss of subtelomeric sequence associated with a terminal inversion duplication of the short arm of chromosome 4.

    Cotter PD, Kaffe S, Li L, Gershin IF, Hirschhorn K.

    Am J Med Genet. 2001 Jul 22;102(1):76-80.PMID: 11471177 [PubMed - indexed for MEDLINE]Related articles

    17.

    D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p).

    Minelli A, Floridia G, Rossi E, Clementi M, Tenconi R, Camurri L, Bernardi F, Hoeller H, Previde Re C, Maraschio P, et al.

    Hum Genet. 1993 Oct;92(4):391-6.PMID: 7901142 [PubMed - indexed for MEDLINE]Related articles

    18.

    Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques.

    de Pater JM, Govaerts LC, de Man SA, van der Sijs-Bos CJ, Christiaens GC, van Dam WM, Loneus WH, Engelen JJ.

    Prenat Diagn. 2003 Sep;23(9):747-51.PMID: 12975787 [PubMed - indexed for MEDLINE]Related articles

    19.

    Molecular topography of the secondary constriction region (qh) of human chromosome 9 with an unusual euchromatic band.

    Verma RS, Luke S, Brennan JP, Mathews T, Conte RA, Macera MJ.

    Am J Hum Genet. 1993 May;52(5):981-6.PMID: 8488847 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.

    Zhang L, Parkhurst JB, Kern WF, Scott KV, Niccum D, Mulvihill JJ, Li S.

    Chin Med J (Engl). 2003 Sep;116(9):1298-303.PMID: 14527352 [PubMed - indexed for MEDLINE]Related articlesFree article

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