BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 7923860)

  • 1. 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]  

  • 2. De novo isochromosome 18p in a female dysmorphic child.
    Ramegowda S; Gawde HM; Hyderi A; Savitha MR; Patel ZM; Krishnamurthy B; Ramachandra NB
    J Appl Genet; 2006; 47(4):397-401. PubMed ID: 17132906
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Clinical outcome: a monosomy 18p is better than a tetrasomy 18p.
    Wei J; Xie Y; He W; Liu W; Jian W; Chen M; Wang D; Wang X; Sun X
    Cytogenet Genome Res; 2014; 144(4):294-8. PubMed ID: 25634515
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. Constitutional tetrasomy 18p.
    Bakshi SR; Brahmbhatt MM; Trivedi PJ; Chudoba I
    Indian Pediatr; 2006 Apr; 43(4):357-60. PubMed ID: 16651677
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The clinical spectrum of a rare chromosomal abnormality: Isochromosome 18p.
    Nur BG; Clark OA; Cetin Z; Toylu A; Karauzum SB; Mihci E
    Genet Couns; 2016; 27(2):223-31. PubMed ID: 29485826
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Confirmation of isochromosome 18p using whole chromosome arm-specific fluorescence in situ hybridization.
    Mewar R; Harrison W; Overhauser J
    Cytogenet Cell Genet; 1993; 64(1):1-4. PubMed ID: 8508672
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A patient with isochromosome 18q, radial-thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocation.
    Sahoo T; Naeem R; Pham K; Chheng S; Noblin ST; Bacino CA; Gambello MJ
    Am J Med Genet A; 2005 Feb; 133A(1):93-8. PubMed ID: 15637724
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tetrasomy 18p in two cases confirmation by in situ hybridization.
    Esmer MC; Frias S; Gómez L; Carnevale A
    Ann Genet; 1994; 37(3):156-9. PubMed ID: 7847800
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Prenatal diagnosis of tetrasomy 18p using multiplex fluorescent PCR and comparison with a variety of techniques.
    Irwin DL; Bryan JL; Chan FY; Matthews PL; Healey SC; Peters M; Findlay I
    Genet Test; 2003; 7(1):1-6. PubMed ID: 12820695
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A case with a rare chromosomal abnormality: isochromosome 18p.
    Dundar M; Caglayan AO; Saatci C; Cetin Z; Arslan K; Uzak AS
    Genet Couns; 2010; 21(1):69-74. PubMed ID: 20420032
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.
    Darnaude MT; Diaz de Bustamante A; Cabello P; Vallcorba I
    Ann Genet; 1996; 39(2):61-3. PubMed ID: 8766134
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sibs with tetrasomy 18p born to a mother with trisomy 18p.
    Takeda K; Okamura T; Hasegawa T
    J Med Genet; 1989 Mar; 26(3):195-7. PubMed ID: 2651671
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome.
    Chen CP; Ko TM; Chen YY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):836-839. PubMed ID: 29241930
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. A new case of "complete" trisomy 5p with isochromosome 5p associated with a de novo translocation t(5;8)(q11;p23).
    Fujita M; Flori E; Lemaire F; Casanova R; Astruc D
    Clin Genet; 1994 Jun; 45(6):305-7. PubMed ID: 7923861
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.