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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 9154131)

  • 1. Characterization of a de novo unbalanced chromosome rearrangement by comparative genomic hybridization and fluorescence in situ hybridization.
    Levy B; Gershin IF; Desnick RJ; Babu A; Gelb BD; Hirschhorn K; Cotter PD
    Cytogenet Cell Genet; 1997; 76(1-2):68-71. PubMed ID: 9154131
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of two add(4qter) chromosomes by comparative genomic hybridization.
    Bocéno M; Rival JM; Nomballais MF; David A; Avet-Loiseau H
    Ann Genet; 1998; 41(2):83-6. PubMed ID: 9706338
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotype.
    Erdel M; Duba HC; Verdorfer I; Lingenhel A; Geiger R; Gutenberger KH; Ludescher E; Utermann B; Utermann G
    Hum Genet; 1997 May; 99(5):596-601. PubMed ID: 9150724
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocation.
    Chen CP; Lin SP; Hsu CH; Chern SR; Su JW; Chen YJ; Pan CW; Wang W
    Genet Couns; 2012; 23(2):223-9. PubMed ID: 22876581
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification and characterization of a de novo partial trisomy 10p by comparative genomic hybridization (CGH).
    Benzacken B; Lapierre JM; Siffroi JP; Chalvon A; Tachdjian G
    Clin Genet; 1998 Oct; 54(4):334-40. PubMed ID: 9831346
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
    Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
    Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies.
    Celep F; Acar H; Aynaci O; Aynaci FM; Karagüzel A
    Genet Couns; 2001; 12(4):319-26. PubMed ID: 11837600
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two further cases of WHS with unbalanced de novo translocation t(4;8) characterised by CGH and FISH.
    Tönnies H; Stumm M; Neumann L; Volleth M; Grumpelt U; Müsebeck J; Annuss G; Neitzel H
    J Med Genet; 2001 Jun; 38(6):E21. PubMed ID: 11389168
    [No Abstract]   [Full Text] [Related]  

  • 10. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
    Mark HF; Wyandt H; Huang XL; Milunsky JM
    Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.
    Dawson AJ; Mears AJ; Chudley AE; Bech-Hansen T; McDermid H
    J Med Genet; 1996 Nov; 33(11):952-6. PubMed ID: 8950677
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
    Shaffer LG; Spikes AS; Macha M; Dunn R
    J Reprod Med; 1996 May; 41(5):367-71. PubMed ID: 8725766
    [TBL] [Abstract][Full Text] [Related]  

  • 14. De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21.
    Riegel M; Baumer A; Piram A; Ortolan D; Peres LC; Pina-Neto JM
    Genet Couns; 2001; 12(1):69-75. PubMed ID: 11332980
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comparative genomic hybridization-aided unraveling of complex karyotypes in human hematopoietic neoplasias.
    Verdorfer I; Brecevic L; Saul W; Schenker B; Kirsch M; Trautmann U; Helm G; Gramatzki M; Gebhart E
    Cancer Genet Cytogenet; 2001 Jan; 124(1):1-6. PubMed ID: 11165314
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement.
    Preiksaitiene E; Benušienė E; Ciuladaite Z; Šliužas V; Mikštienė V; Kučinskas V
    Taiwan J Obstet Gynecol; 2016 Jun; 55(3):410-4. PubMed ID: 27343325
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization.
    Cain CC; Saul D; Attanasio L; Oehler E; Hamosh A; Blakemore K; Stetten G
    Prenat Diagn; 2007 Apr; 27(4):373-9. PubMed ID: 17286317
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
    Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
    J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
    Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization.
    Tosi S; Giudici G; Rambaldi A; Scherer SW; Bray-Ward P; Dirscherl L; Biondi A; Kearney L
    Genes Chromosomes Cancer; 1999 Mar; 24(3):213-21. PubMed ID: 10451701
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.