BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

292 related articles for article (PubMed ID: 2077349)

  • 1. Evidence for involvement of a Robertsonian translocation 13 chromosome in formation of a ring chromosome 13.
    Stetten G; Tuck-Muller CM; Blakemore KJ; Wong C; Kazazian HH; Antonarakis SE
    Mol Biol Med; 1990 Dec; 7(6):479-84. PubMed ID: 2077349
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. Trisomy/partial monosomy 13 mosaicism associated with relatively mild clinical malformation.
    Duckett DP; Porter HJ; Young ID
    Ann Genet; 1992; 35(2):113-6. PubMed ID: 1524408
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11).
    Fryns JP; Kleczkowska A
    Ann Genet; 1987; 30(2):109-10. PubMed ID: 3499841
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Prenatal diagnosis of mosaic tetrasomy 5p.
    Park JP; Barefoot KH; Ornvold K; Berg SZ; Dossu JR; Mohandas TK
    Prenat Diagn; 2001 May; 21(5):351-3. PubMed ID: 11360274
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.
    Coêlho KE; Egashira M; Kato R; Fujimoto M; Matsumoto N; Rerkamnuaychoke B; Abe K; Harada N; Ohashi H; Fukushima Y; Niikawa N
    Am J Med Genet; 1996 Jun; 63(3):468-71. PubMed ID: 8737654
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Extra-small marker chromosomes in couples with reproductive failure.
    Ioan D; Dumitriu L; Ghergar D; Belengeanu V; Soare GH; Maximilian C
    Endocrinologie; 1987; 25(1):41-3. PubMed ID: 3472313
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Complex rearrangement of chromosomes 3 and 5 in an adolescent with multiple abnormalities].
    Naffah J; Der Kaloustian V
    Ann Genet; 1975 Jun; 18(2):121-4. PubMed ID: 242250
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS; Hegmann K; Smith JL; Shaffer LG
    Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis.
    Wang H; McLaughlin M; Thompson C; Hunter AG
    Am J Med Genet; 1993 Jun; 46(5):559-62. PubMed ID: 8322821
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [The clinical picture of 13q22-qter duplication in a 2-year-old boy].
    Halasová E; Lukácová M; Bergendiová E; Kamenická E
    Cesk Pediatr; 1987 Aug; 42(8):477-9. PubMed ID: 3664759
    [No Abstract]   [Full Text] [Related]  

  • 14. Maternal uniparental disomy for chromosome 14 in a boy with intrauterine growth retardation.
    Miyoshi O; Hayashi S; Fujimoto M; Tomita H; Sohda M; Niikawa N
    J Hum Genet; 1998; 43(2):138-42. PubMed ID: 9621521
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Duplication (17p) in a child with an isodicentric (17p) chromosome.
    Mascarello JT; Jones MC; Hoyme HE; Freebury MM
    Am J Med Genet; 1983 Jan; 14(1):67-72. PubMed ID: 6681937
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
    Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ring chromosome 2 in a child with growth failure and few congenital abnormalities.
    Vigfusson NV; Kapstafer KJ; Lloyd MA
    Am J Med Genet; 1980; 7(3):383-9. PubMed ID: 7468662
    [TBL] [Abstract][Full Text] [Related]  

  • 18. De novo partial 2p duplication with postmortem description.
    Monteleone PL; Blair JD; Graviss ER; Chen SC; Salvador A; Grzegocki JA; Monteleone JA
    Am J Med Genet; 1981; 10(1):55-64. PubMed ID: 7197468
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours].
    Steinborn A; Röddiger S; Born HJ; Baier P; Halberstadt E
    Z Geburtshilfe Neonatol; 1996; 200(5):186-90. PubMed ID: 9035828
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia.
    Hatem E; Meriam BR; Walid D; Adenen M; Moez G; Ali S
    Prenat Diagn; 2007 May; 27(5):471-4. PubMed ID: 17380471
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.