These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

78 related articles for article (PubMed ID: 8494038)

  • 1. Method for sequential staining of GTL-banded metaphases with fluorescent-labeled chromosome-specific paint probes.
    Jalal SM; Law ME; Christensen ER; Spurbeck JL; Dewald GW
    Am J Med Genet; 1993 Apr; 46(1):98-103. PubMed ID: 8494038
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.
    Lorentz CP; Jalal SM; Thompson DM; Babovic-Vuksanovic D
    Am J Med Genet; 2002 Jul; 111(1):61-7. PubMed ID: 12124737
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sequential G-banding and fluorescent in situ hybridization on peripheral blood, bone marrow, and amniotic fluid samples.
    Wiktor A; Puskorius R; Zubrickas K; Van Dyke DL
    Am J Med Genet; 1998 Aug; 79(1):38-41. PubMed ID: 9738867
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Y chromosome heterochromatin of differing lengths in two cell populations of the same individual.
    Akkari Y; Lawce H; Kelson S; Smith C; Davis C; Boyd L; Magenis RE; Olson S
    Prenat Diagn; 2005 Apr; 25(4):304-6. PubMed ID: 15849801
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.
    Schoch C; Haferlach T; Bursch S; Gerstner D; Schnittger S; Dugas M; Kern W; Löffler H; Hiddemann W
    Genes Chromosomes Cancer; 2002 Sep; 35(1):20-9. PubMed ID: 12203786
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fetoplacental discrepancy involving structural abnormalities of chromosome 8 detected by prenatal diagnosis.
    Soler A; Sánchez A; Carrió A; Badenas C; Milà M; Borrell A
    Prenat Diagn; 2003 Apr; 23(4):319-22. PubMed ID: 12673638
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Chromosome analysis of 1133 cases in genetic counseling clinic].
    Zhao Y; Liu CY; Cheng ZY; Ye LZ; Gao CS; Ma SW; Zhang JC; Shi HP; Yuan LF; Luo HY
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1987 Jun; 9(3):157-64. PubMed ID: 2958156
    [No Abstract]   [Full Text] [Related]  

  • 9. Tetrasomy 12p--unusual presentation in CVS.
    Dong L; Falk RE; Williams J; Kohan M; Schreck RR
    Prenat Diagn; 2003 Feb; 23(2):101-3. PubMed ID: 12575013
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A partial trisomy 15q due to 15;17 translocation detected by conventional cytogenetic and FISH techniques.
    Cora T; Acar H; Oran B
    Genet Couns; 2000; 11(1):25-32. PubMed ID: 10756424
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Application of chromosome painting to analysis of structural aberration in five cases].
    Su G; Qiao H; Shi Z; Su R; Zeng X; Zhao F; Yang H; Huang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Aug; 15(4):202-5. PubMed ID: 9691125
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A new chromosome banding technique, spectral color banding (SCAN), for full characterization of chromosomal abnormalities.
    Kakazu N; Bar-Am I; Hada S; Ago H; Abe T
    Genes Chromosomes Cancer; 2003 Aug; 37(4):412-6. PubMed ID: 12800153
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A patient with myelodysplastic syndrome studied by GTG-banding and fluorescent in situ hybridization (FISH).
    Mark HF; Mark Y; Sotomayor E; Sambandam S
    Cytobios; 1998; 94(376):121-8. PubMed ID: 9839434
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spectral karyotyping analysis of head and neck squamous cell carcinoma.
    Singh B; Gogineni S; Goberdhan A; Sacks P; Shaha A; Shah J; Rao P
    Laryngoscope; 2001 Sep; 111(9):1545-50. PubMed ID: 11568603
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chimerism and multiple numerical chromosome imbalances in a spontaneously aborted fetus.
    Vorsanova SG; Iourov IY; Demidova IA; Kirillova EA; Soloviev IV; Yurov YB
    Tsitol Genet; 2006; 40(5):28-30. PubMed ID: 17385415
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome.
    Kakazu N; Taniwaki M; Horiike S; Nishida K; Tatekawa T; Nagai M; Takahashi T; Akaogi T; Inazawa J; Ohki M; Abe T
    Genes Chromosomes Cancer; 1999 Dec; 26(4):336-45. PubMed ID: 10534769
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytogenetic and molecular analysis in trisomy 12p.
    Allen TL; Brothman AR; Carey JC; Chance PF
    Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Detection of t(15;17) using cytogenetic, fluorescent in situ hybridization, and molecular techniques. Comparative study of 11 patients with acute promyelocytic leukemia].
    Arranz E; Robledo M; Martínez B; Prieto E; Román A; Benítez J
    Sangre (Barc); 1997 Feb; 42(1):11-5. PubMed ID: 9229797
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.