BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 1488982)

  • 1. Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with alpha-satellite DNA probes: detection of a centromeric DNA break?
    Cantú ES; Khan TA; Pai GS
    Am J Med Genet; 1992 Oct; 44(3):340-4. PubMed ID: 1488982
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Analysis of a whole arm translocation between chromosomes 18 and 20 using fluorescence in situ hybridization: detection of a break in the centromeric alpha-satellite sequences.
    Tümer Z; Berg A; Mikkelsen M
    Hum Genet; 1995 Mar; 95(3):299-302. PubMed ID: 7868122
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Centromeric alpha-satellite DNA break in reciprocal translocations.
    Wang JC; Hajianpour A; Habibian R
    Cytogenet Genome Res; 2009; 125(4):329-33. PubMed ID: 19864896
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p.
    Wang JC; Nemana L; Kou SY; Habibian R; Hajianpour MJ
    Am J Med Genet; 1997 Sep; 71(4):463-6. PubMed ID: 9286456
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Non-radioactive in situ hybridization of alpha-satellite sequences in cytogenetic diagnosis].
    Perfumo C; Arslanian A; Zara F; Piombo G; Pierluigi M
    Pathologica; 1992; 84(1091):363-9. PubMed ID: 1465321
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16.
    Wang JC; Mamunes P; Kou SY; Schmidt J; Mao R; Hsu WT
    Am J Med Genet; 1998 Dec; 80(4):418-22. PubMed ID: 9856575
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
    Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J
    Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.
    McGhee EM; Qu Y; Wohlferd MM; Goldberg JD; Norton ME; Cotter PD
    Clin Genet; 2001 Apr; 59(4):274-8. PubMed ID: 11298684
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Detection or exclusion of fetal trisomy 18 by in-situ-hybridization of the histologic section].
    Wille S; Mehraein Y
    Geburtshilfe Frauenheilkd; 1993 Oct; 53(10):684-8. PubMed ID: 8270150
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of an unusual marker chromosome by spectral karyotyping.
    Huang B; Ning Y; Lamb AN; Sandlin CJ; Jamehdor M; Ried T; Bartley J
    Am J Med Genet; 1998 Dec; 80(4):368-72. PubMed ID: 9856565
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dual-color fish analysis of breakpoints on Robertsonian translocations.
    Takahashi Y; Fujita H; Nakamura Y; Kurahashi H
    Jpn J Hum Genet; 1997 Dec; 42(4):517-23. PubMed ID: 9560951
    [TBL] [Abstract][Full Text] [Related]  

  • 14. False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite DNA probe (D18Z1) to the heterochromatic region of chromosome 9.
    Wei S; Siu VM; Decker A; Quigg MH; Roberson J; Xu J; Adeyinka A
    Prenat Diagn; 2007 Nov; 27(11):1064-6. PubMed ID: 17654752
    [No Abstract]   [Full Text] [Related]  

  • 15. [Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization].
    Solov'ev IV; Iurov IuB; Vorsanova SG; Marcais B; Rogaev EI; Kapanadze BI; Brodianskiĭ VM; Iankovskiĭ NK; Roizes G
    Genetika; 1998 Nov; 34(11):1470-9. PubMed ID: 10096024
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 18p monosomy with midline defects and a de novo satellite identified by FISH.
    Taine L; Goizet C; Wen ZQ; Chateil JF; Battin J; Saura R; Lacombe D
    Ann Genet; 1997; 40(3):158-63. PubMed ID: 9401105
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. Keratosis pilaris and ulerythema ophryogenes associated with an 18p deletion caused by a Y/18 translocation.
    Nazarenko SA; Ostroverkhova NV; Vasiljeva EO; Nazarenko LP; Puzyrev VP; Malet P; Nemtseva TA
    Am J Med Genet; 1999 Jul; 85(2):179-82. PubMed ID: 10406673
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Centromeric association of chromosome 16- and 18-derived microchromosomes.
    Felbor U; Rutschow D; Haaf T; Schmid M
    Hum Genet; 2002 Jul; 111(1):16-25. PubMed ID: 12136231
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.