BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 1863990)

  • 1. Molecular identification of a small supernumerary marker chromosome by in situ hybridization: diagnosis of an isochromosome 18p with probe L1.84.
    Blennow E; Nielsen KB
    Clin Genet; 1991 Jun; 39(6):429-33. PubMed ID: 1863990
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization.
    Callen DF; Freemantle CJ; Ringenbergs ML; Baker E; Eyre HJ; Romain D; Haan EA
    Am J Hum Genet; 1990 Sep; 47(3):493-8. PubMed ID: 2393023
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Isodicentric chromosome 18 in an abnormal infant using chromosome specific DNA probe.
    Meguid NA; Habibian R
    Clin Genet; 1992 May; 41(5):225-8. PubMed ID: 1606710
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
    Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Diagnosis of tetrasomy 18p using in situ hybridization of a DNA probe to metaphase chromosomes.
    Park VM; Gustashaw KM; Bilenker RM; Golden WL
    Am J Med Genet; 1991 Nov; 41(2):180-3. PubMed ID: 1785630
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of a supernumerary der(18) chromosome by a rational strategy for the cytogenetic typing of small marker chromosomes with chromosome-specific DNA probes.
    Koch J; Fischer H; Askholm H; Hindkjaer J; Pedersen S; Kølvraa S; Bolund L
    Clin Genet; 1993 Apr; 43(4):200-3. PubMed ID: 8330453
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing.
    Eggermann T; Engels H; Moskalonek B; Nöthen MM; Müller-Navia J; Schleiermacher E; Schwanitz G; Stengel-Rutkowski S
    Hum Genet; 1996 May; 97(5):568-72. PubMed ID: 8655132
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Isochromosome 18p in a mother and her child.
    Abeliovich D; Dagan J; Levy A; Steinberg A; Zlotogora J
    Am J Med Genet; 1993 Jun; 46(4):392-3. PubMed ID: 8357009
    [TBL] [Abstract][Full Text] [Related]  

  • 9. De novo isochromosome 18p in two patients: cytogenetic diagnosis and confirmation by chromosome painting.
    Back E; Toder R; Voiculescu I; Wildberg A; Schempp W
    Clin Genet; 1994 Jun; 45(6):301-4. PubMed ID: 7923860
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.
    Levy B; Papenhausen P; Tepperberg J; Dunn T; Fallet S; Magid M; Kardon N; Hirschhorn K; Warburton P
    Cytogenet Cell Genet; 2000; 91(1-4):165-70. PubMed ID: 11173851
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of an extranumerary i(22p) with normal phenotype.
    Doneda L; Dalprà L; Tibiletti MG; Larizza L
    Ann Genet; 1993; 36(3):154-8. PubMed ID: 8117060
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The origin of a morphologically unidentifiable human supernumerary minichromosome traced through sorting, molecular cloning, and in situ hybridisation.
    Raimondi E; Ferretti L; Young BD; Sgaramella V; De Carli L
    J Med Genet; 1991 Feb; 28(2):92-6. PubMed ID: 2002493
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication.
    Moog U; Engelen JJ; de Die-Smulders CE; Albrechts JC; Loneus WH; Haagen AA; Raven EJ; Hamers AJ
    Clin Genet; 1994 Dec; 46(6):423-9. PubMed ID: 7889659
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of marker chromosomes in thirteen patients using FISH probing.
    Daniel A; Malafiej P; Preece K; Chia N; Nelson J; Smith M
    Am J Med Genet; 1994 Oct; 53(1):8-18. PubMed ID: 7802042
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
    In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of iso(18p) marker chromosome by fluorescence in situ hybridization with single-copy DNA probe.
    Nakashima H; Hasegawa T; Sakai M; Inaba R; Imamura T
    Jpn J Hum Genet; 1995 Jun; 40(2):185-8. PubMed ID: 7662998
    [TBL] [Abstract][Full Text] [Related]  

  • 17. DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome.
    Mattei MG; Philip N; Passage E; Moisan JP; Mandel JL; Mattei JF
    Hum Genet; 1985; 69(3):268-71. PubMed ID: 3980018
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Non-radioactive in situ hybridization with chromosome-specific probes].
    Bryndorf TE; Christensen B; Philip J
    Ugeskr Laeger; 1992 May; 154(21):1487-91. PubMed ID: 1598719
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Trisomy 18p caused by a supernumerary marker with a chromosome 13/21 centromere: a possible recurrent chromosome aberration.
    Plaja A; Lloveras E; Martinez-Bouzas C; Barreña B; Del Campo M; Fernández A; Herrero M; Barranco L; Palau N; López-Aríztegui MA; Català V; Tejada MI
    Am J Med Genet A; 2013 Sep; 161A(9):2363-8. PubMed ID: 23894094
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.
    Tharapel AT; Qumsiyeh MB; Martens PR; Tharapel SA; Dalton JD; Ward JC; Wilroy RS
    Am J Med Genet; 1991 Jul; 40(1):117-20. PubMed ID: 1887840
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.