BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 17132906)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Tetrasomy 18p de novo: parental origin and different mechanisms of formation.
    Bugge M; Blennow E; Friedrich U; Petersen MB; Pedeutour F; Tsezou A; Orum A; Hermann S; Lyngbye T; Sarri C; Avramopoulos D; Kitsiou S; Lambert JC; Guzda M; Tommerup N; Brøndum-Nielsen K
    Eur J Hum Genet; 1996; 4(3):160-7. PubMed ID: 8840116
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 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. Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literature.
    Eggermann T; Schubert R; Engels H; Apacik C; Stengel-Rutkowski S; Haefliger C; Emiliani V; Ricagni C; Schwanitz G
    Ann Genet; 1999; 42(2):75-80. PubMed ID: 10434120
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Grandmaternal origin of an isochromosome 18p present in two maternal half-sisters.
    Boyle J; Sangha K; Dill F; Robinson WP; Yong SL
    Am J Med Genet; 2001 Jun; 101(1):65-9. PubMed ID: 11343341
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formation.
    van den Berg C; Pijpers L; Halley DJ; Opstal DV; Los FJ
    Am J Med Genet; 1999 Sep; 86(2):151-5. PubMed ID: 10449651
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Different conformation of two supernumerary 18p isochromosomes, one with a concomitant partial 18q trisomy.
    Noronha Dutra AR; Mancini TI; Satomi Takeno S; Moysés Oliveira M; Kim CA; Alvarez Perez AB; Domenici Kulikowski L; Melaragno MI
    Cytogenet Genome Res; 2012; 138(1):1-4. PubMed ID: 22796746
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Isochromosome 18p results from maternal meiosis II nondisjunction.
    Kotzot D; Bundscherer G; Bernasconi F; Brecevic L; Lurie IW; Basaran S; Baccicchetti C; Höller A; Castellan C; Braun-Quentin C; Pfeiffer RA; Schinzel A
    Eur J Hum Genet; 1996; 4(3):168-74. PubMed ID: 8840117
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
    Oner G; Jauch A; Eggermann T; Hardwick R; Kirsch S; Schiebel K; Rappold G; Robson L; Smith A
    Am J Med Genet; 2000 May; 92(2):101-6. PubMed ID: 10797432
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Co-occurrence of mosaic supernumerary isochromosome 18p and intermittent 2q13 deletions in a child with multiple congenital anomalies.
    Jaiswal SK; Kumar A; Ali A; Rai AK
    Gene; 2015 Mar; 559(1):94-8. PubMed ID: 25617521
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome.
    Lee JH; Cho HS; Lee ES; Jung BC
    Korean J Lab Med; 2010 Jun; 30(3):312-7. PubMed ID: 20603594
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.