These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


201 related items for PubMed ID: 8160749

  • 1. Confirmation of proximal 1q duplication using fluorescence in situ hybridization.
    Chen H, Kusyk CJ, Tuck-Muller CM, Martinez JE, Dorand RD, Wertelecki W.
    Am J Med Genet; 1994 Mar 01; 50(1):28-31. PubMed ID: 8160749
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorhic features.
    Rao VB, Kerketta L, Korgaonkar S, Ghosh K, Mohanty D.
    Genet Couns; 2005 Mar 01; 16(2):139-43. PubMed ID: 16082769
    [Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR, Huff RW, Ridgway LE, Stratton RF, Moore CM.
    Am J Med Genet; 1994 Mar 01; 50(1):21-7. PubMed ID: 8160748
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13).
    Tschernigg M, Petek E, Leonhardtsberger A, Wagner K, Kroisel PM.
    Genet Couns; 2002 Mar 01; 13(3):303-7. PubMed ID: 12416638
    [Abstract] [Full Text] [Related]

  • 9. Boy with an interstitial 1q (q31q41) duplication confirmed by fluorescent in situ hybridisation.
    Sillén A, Wadelius C, Annerén G.
    Am J Med Genet; 1998 Nov 02; 80(2):163-8. PubMed ID: 9805135
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Small inherited terminal duplication of 7q with hydrocephalus, cleft palate, joint contractures, and severe hypotonia.
    Morava E, Bartsch O, Czakó M, Frensel A, Kalscheuer V, Kárteszi J, Kosztolányi G.
    Clin Dysmorphol; 2003 Apr 02; 12(2):123-7. PubMed ID: 12868476
    [Abstract] [Full Text] [Related]

  • 15. Characterization of a derivative chromosome 17 by fish-technique.
    Ramesh KH, Shah HO, Sherman J, Lin JH, Verma RS.
    Ann Genet; 1996 Apr 02; 39(3):177-80. PubMed ID: 8839891
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. 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 02; 8(2):91-7. PubMed ID: 9219006
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
    Ito M, Mutoh K, Okuno T, Mikawa H, Edagawa J, Abe T.
    Ann Genet; 1983 Apr 02; 26(2):116-9. PubMed ID: 6604486
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 11.