BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

252 related articles for article (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; 52(2):214-7. PubMed ID: 7802011
    [TBL] [Abstract][Full Text] [Related]  

  • 2. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
    Legare JM; Sekhon GS; Laxova R
    Am J Med Genet; 1994 Nov; 53(3):216-21. PubMed ID: 7856655
    [TBL] [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; 44(4):477-81. PubMed ID: 1442891
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Unbalanced mosaic karyotypes with different structural abnormalities involving a common chromosome region: report of two cases.
    Pettenati MJ; Teot LA; Smith C; Hayworth R; Thomas IT; Veille JC; Rao PN
    Am J Med Genet; 1993 Feb; 45(3):365-9. PubMed ID: 8434625
    [TBL] [Abstract][Full Text] [Related]  

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

  • 6. Mosaicism with a normal cell line and an unbalanced structural rearrangement.
    Zaslav AL; Fallet S; Blumenthal D; Jacob J; Fox J
    Am J Med Genet; 1999 Jan; 82(1):15-9. PubMed ID: 9916836
    [TBL] [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; 4(1):37-41. PubMed ID: 8471219
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characterization of a derivative chromosome 17 by fish-technique.
    Ramesh KH; Shah HO; Sherman J; Lin JH; Verma RS
    Ann Genet; 1996; 39(3):177-80. PubMed ID: 8839891
    [TBL] [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; 32(3):177-9. PubMed ID: 2486064
    [TBL] [Abstract][Full Text] [Related]  

  • 10. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
    Merlob P; Kohn G; Litwin A; Nissenkorn I; Katznelson MB; Reisner SH
    Am J Med Genet; 1989 Jan; 32(1):22-6. PubMed ID: 2705479
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
    Syrrou M; Borghgraef M; Fryns JP
    Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 18q- and 18q+ mosaicism in a mentally retarded boy.
    Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
    Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complex chromosome rearrangements and congenital anomalies.
    Kousseff BG; Nichols P; Essig YP; Miller K; Weiss A; Tedesco TA
    Am J Med Genet; 1987 Apr; 26(4):771-82. PubMed ID: 3591822
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Unusual mosaic trisomy 13 through 13/13 translocation and monosomy 13 with a small ring.
    Jalal SM; Martin JA; Benjamin TR; Kukolich MK; Townsend-Parcham JK
    Ann Genet; 1990; 33(3):173-5. PubMed ID: 2288463
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial deletion of 18p and partial duplication of 18q caused by a paternal pericentric inversion.
    Israƫls T; Hoovers J; Turpijn HM; Wijburg FA; Hennekam RC
    Clin Genet; 1996 Dec; 50(6):520-4. PubMed ID: 9147887
    [TBL] [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; 21(2):69-71. PubMed ID: 15017469
    [TBL] [Abstract][Full Text] [Related]  

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

  • 18. Duplication of distal 22q.
    Abeliovich D; Maor E; Bashan N; Carmi R
    Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354
    [TBL] [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; 29(7):503-6. PubMed ID: 1640434
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.
    Prabhakara K; Wyandt HE; Huang XL; Prasad KS; Ramadevi AR
    Ann Genet; 2004; 47(3):297-303. PubMed ID: 15337476
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.