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

PUBMED FOR HANDHELDS

Journal Abstract Search

249 related items for PubMed ID: 7802011

  • 1. Jumping translocation in a newborn boy with dup(4q) and severe hydrops fetalis.
    Duval E, van den Enden A, Vanhaesebrouck P, Speleman F.
    Am J Med Genet; 1994 Aug 15; 52(2):214-7. PubMed ID: 7802011
    [Abstract] [Full Text] [Related]

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

  • 3. Confirmation of a cryptic unbalanced translocation using whole chromosome fluorescence in situ hybridization.
    Mewar R, Kline AD, Jackson L, Overhauser J.
    Am J Med Genet; 1992 Nov 01; 44(4):477-81. PubMed ID: 1442891
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Translocation/duplication of 9p onto a duplicated 4q.
    Rivera H, Figuera LE, Vasquez AI.
    Genet Couns; 1992 Nov 01; 3(4):201-3. PubMed ID: 1472355
    [Abstract] [Full Text] [Related]

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

  • 7. Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p.
    Fryns JP, Kleczkowska A, Devriendt K, Devliegher H, Van den Berghe H.
    Genet Couns; 1993 Nov 01; 4(1):37-41. PubMed ID: 8471219
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
    Fryns JP, Kleczkowska A, Jaeken J, Van Herck K, Van den Berghe MH.
    Ann Genet; 1989 Nov 01; 32(3):177-9. PubMed ID: 2486064
    [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.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Partial deletion of 18p and partial duplication of 18q caused by a paternal pericentric inversion.
    Israëls T, Hoovers J, Turpijn HM, Wijburg FA, Hennekam RC.
    Clin Genet; 1996 Dec 01; 50(6):520-4. PubMed ID: 9147887
    [Abstract] [Full Text] [Related]

  • 16. A dysmorphic newborn infant with a complex rearrangement involving chromosomes 2, 4, and 6 detected by fluorescence in situ hybridization (FISH).
    Hoffman DJ, Punnett HH, Pyeritz RE.
    Am J Perinatol; 2004 Feb 01; 21(2):69-71. PubMed ID: 15017469
    [Abstract] [Full Text] [Related]

  • 17. Isochromosome-formation in chromosome 9.
    Miller K, Arslan-Kirchner M.
    Ann Genet; 1994 Feb 01; 37(2):78-81. PubMed ID: 7985983
    [Abstract] [Full Text] [Related]

  • 18. Duplication of distal 22q.
    Abeliovich D, Maor E, Bashan N, Carmi R.
    Am J Med Genet; 1989 Mar 01; 32(3):346-9. PubMed ID: 2729354
    [Abstract] [Full Text] [Related]

  • 19. Necropsy findings in a fetus with a 46,XY,dic t(X;21)(p11.1;p11.1).
    Smith NM, Fernandez H, Chambers HM, Callen DF.
    J Med Genet; 1992 Jul 01; 29(7):503-6. PubMed ID: 1640434
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.