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Journal Abstract Search

193 related items for PubMed ID: 8533837

  • 1. Four new cases of inverted terminal duplication: a modified hypothesis of mechanism of origin.
    Hoo JJ, Chao M, Szego K, Rauer M, Echiverri SC, Harris C.
    Am J Med Genet; 1995 Sep 25; 58(4):299-304. PubMed ID: 8533837
    [Abstract] [Full Text] [Related]

  • 2. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.
    de Die-Smulders CE, Engelen JJ, Schrander-Stumpel CT, Govaerts LC, de Vries B, Vles JS, Wagemans A, Schijns-Fleuren S, Gillessen-Kaesbach G, Fryns JP.
    Am J Med Genet; 1995 Nov 20; 59(3):369-74. PubMed ID: 8599364
    [Abstract] [Full Text] [Related]

  • 3. Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8.
    Barber JC, James RS, Patch C, Temple IK.
    Am J Med Genet; 1994 Apr 15; 50(3):296-9. PubMed ID: 8042676
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  • 5. Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion.
    Knijnenburg J, van Haeringen A, Hansson KB, Lankester A, Smit MJ, Belfroid RD, Bakker E, Rosenberg C, Tanke HJ, Szuhai K.
    Eur J Hum Genet; 2007 May 15; 15(5):548-55. PubMed ID: 17342151
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  • 8. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS, Gibson L, McGrath J, Meyn MS, Breg WR, Yang-Feng TL.
    Am J Med Genet; 1993 May 15; 46(3):288-92. PubMed ID: 8488873
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  • 9. [Inverted duplication of the short arm of chromosome 8].
    Rodríguez Martínez L, Jiménez Muñoz-Delgado N, Nieto C, Martínez Carrascal A, López Grondona F, Martínez Frías ML.
    An Esp Pediatr; 2001 Nov 15; 55(5):458-62. PubMed ID: 11696311
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  • 10. Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
    Zenger-Hain JL, Van Dyke DL, Wiktor A, Walker H, Feldman GL.
    Am J Med Genet; 1993 Dec 01; 47(8):1198-201. PubMed ID: 8291556
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  • 11. [Cytogenetic and molecular genetic study of a case with 8p inverted duplication deletion syndrome].
    Han X, Zhang JM, Jiang WT, Hu Q, Tao J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug 01; 27(4):361-6. PubMed ID: 20677137
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  • 12. Duplication 10q confirmed by DNA in situ hybridization.
    Johnson VP, Sutliff WC.
    Am J Med Genet; 1994 Aug 15; 52(2):184-7. PubMed ID: 7802006
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  • 13. Chromosome 10p11.2-p12.2 duplication: report of a patient and review of the literature.
    Mégarbané A, Gosset P, Souraty N, Lapierre JM, Korban R, Zahed L, Samaras L, Vekemans M, Prieur M.
    Am J Med Genet; 2001 Dec 01; 104(3):204-8. PubMed ID: 11754045
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  • 14. Further delineation of 7p trisomy. Case report and review of literature.
    Pallotta R, Dalprà L, Fusilli P, Zuffardi O.
    Ann Genet; 1996 Dec 01; 39(3):152-8. PubMed ID: 8839888
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  • 15. Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.
    Coêlho KE, Egashira M, Kato R, Fujimoto M, Matsumoto N, Rerkamnuaychoke B, Abe K, Harada N, Ohashi H, Fukushima Y, Niikawa N.
    Am J Med Genet; 1996 Jun 14; 63(3):468-71. PubMed ID: 8737654
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  • 16. Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence.
    Lindgren V, Rosinsky B, Chin J, Berry-Kravis E.
    Am J Med Genet; 1994 Jan 01; 49(1):67-73. PubMed ID: 8172253
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  • 17. De novo inverted interstitial ("mirror") duplication of chromosome 8(q13----q24.1) in a liveborn male.
    Donnenfeld AE, Coyne MD, Beauregard LJ.
    Am J Med Genet; 1990 Apr 01; 35(4):529-31. PubMed ID: 2333884
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  • 18. Partial trisomy 15q: report of a patient and literature review.
    Chandler K, Schrander-Stumpel CT, Engelen J, Theunissen P, Fryns JP.
    Genet Couns; 1997 Apr 01; 8(2):91-7. PubMed ID: 9219006
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  • 19. A paternally derived inverted duplication of 7q with evidence of a telomeric deletion.
    Stetten G, Charity LL, Kasch LM, Scott AF, Berman CL, Pressman E, Blakemore KJ.
    Am J Med Genet; 1997 Jan 10; 68(1):76-81. PubMed ID: 8986281
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  • 20. U-type exchange is the most frequent mechanism for inverted duplication with terminal deletion rearrangements.
    Rowe LR, Lee JY, Rector L, Kaminsky EB, Brothman AR, Martin CL, South ST.
    J Med Genet; 2009 Oct 10; 46(10):694-702. PubMed ID: 19293169
    [Abstract] [Full Text] [Related]

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