BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

276 related articles for article (PubMed ID: 25827349)

  • 1. Diagnosis of Fanconi anemia by diepoxybutane analysis.
    Auerbach AD
    Curr Protoc Hum Genet; 2015 Apr; 85():8.7.1-8.7.17. PubMed ID: 25827349
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fanconi anemia and its diagnosis.
    Auerbach AD
    Mutat Res; 2009 Jul; 668(1-2):4-10. PubMed ID: 19622403
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diagnosis of fanconi anemia by diepoxybutane analysis.
    Auerbach AD
    Curr Protoc Hum Genet; 2003 Jul; Chapter 8():Unit 8.7. PubMed ID: 18428345
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DEB test for Fanconi anemia detection in patients with atypical phenotypes.
    Esmer C; Sánchez S; Ramos S; Molina B; Frias S; Carnevale A
    Am J Med Genet A; 2004 Jan; 124A(1):35-9. PubMed ID: 14679584
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Differential diagnosis of Fanconi anemia by nitrogen mustard and diepoxybutane.
    Deviren A; Yalman N; Hacihanefioglu S
    Ann Hematol; 2003 Apr; 82(4):223-7. PubMed ID: 12707724
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutations.
    Dokal I; Chase A; Morgan NV; Coulthard S; Hall G; Mathew CG; Roberts I
    Br J Haematol; 1996 Jun; 93(4):813-6. PubMed ID: 8703809
    [TBL] [Abstract][Full Text] [Related]  

  • 7. International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity.
    Auerbach AD; Rogatko A; Schroeder-Kurth TM
    Blood; 1989 Feb; 73(2):391-6. PubMed ID: 2917181
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Differentiation of Fanconi anemia from aplastic anemia by chromosomal breakage test.
    Hou JW; Wang TR
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(2):121-6. PubMed ID: 9151465
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Preliminary communication: prenatal detection of the Fanconi Anemia gene by cytogenetic methods.
    Auerbach AD; Warburton D; Bloom AD; Chaganti RS
    Am J Hum Genet; 1979 Jan; 31(1):77-81. PubMed ID: 433924
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fanconi anemia screening by diepoxybutane and mitomicin C tests in Korean children with bone marrow failure syndromes.
    Kook H; Cho D; Cho SH; Hong WP; Kim CJ; Park JY; Yoon WS; Ryang DW; Hwang TJ
    J Korean Med Sci; 1998 Dec; 13(6):623-8. PubMed ID: 9886171
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method.
    Auerbach AD; Adler B; Chaganti RS
    Pediatrics; 1981 Jan; 67(1):128-35. PubMed ID: 7243421
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromosome fragility in patients with Fanconi anaemia: diagnostic implications and clinical impact.
    Castella M; Pujol R; Callén E; Ramírez MJ; Casado JA; Talavera M; Ferro T; Muñoz A; Sevilla J; Madero L; Cela E; Beléndez C; de Heredia CD; Olivé T; de Toledo JS; Badell I; Estella J; Dasí Á; Rodríguez-Villa A; Gómez P; Tapia M; Molinés A; Figuera Á; Bueren JA; Surrallés J
    J Med Genet; 2011 Apr; 48(4):242-50. PubMed ID: 21217111
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF.
    Popp I; Punekar M; Telford N; Stivaros S; Chandler K; Minnis M; Castleton A; Higham C; Hopewell L; Gareth Evans D; Raams A; Theil AF; Meyer S; Schindler D
    BMC Med Genet; 2018 Jan; 19(1):7. PubMed ID: 29325523
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Fanconi anemia: cytogenetic diagnosis of 40 cases].
    Porto B; Sousa R; Ponte F; Torgal A; Campilho F; Campos A; Gonçalves C; Barbot J
    Acta Med Port; 2011; 24(3):405-12. PubMed ID: 22015027
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clastogen-induced chromosomal breakage as a marker for first trimester prenatal diagnosis of Fanconi anemia.
    Auerbach AD; Min Z; Ghosh R; Pergament E; Verlinsky Y; Nicolas H; Boué J
    Hum Genet; 1986 May; 73(1):86-8. PubMed ID: 3458668
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chromosomal instability in patients with Fanconi anemia from Serbia.
    Cirković S; Guć-Sćekić M; Vujić D; Mićić D; Skorić D
    Vojnosanit Pregl; 2014 Apr; 71(4):368-72. PubMed ID: 24783417
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical, genetic and cytogenetic study of Fanconi anemia in an Indian population.
    Korgaonkar S; Ghosh K; Vundinti BR
    Hematology; 2010 Feb; 15(1):58-62. PubMed ID: 20132664
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Variable response to the diepoxybutane test in two dizygotic twins with Fanconi's anemia and flow cytometry for diagnosis confirmation.
    Toraldo R; Canino G; Tolone C; D'Avanzo M; Porfirio B; Hoehn H; Schroeder-Kurth T; Pistoia V
    Pediatr Hematol Oncol; 1998; 15(1):45-54. PubMed ID: 9509505
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fanconi anemia: causes and consequences of genetic instability.
    Kalb R; Neveling K; Nanda I; Schindler D; Hoehn H
    Genome Dyn; 2006; 1():218-242. PubMed ID: 18724063
    [TBL] [Abstract][Full Text] [Related]  

  • 20. FANCD2 Western blot as a diagnostic tool for Brazilian patients with Fanconi anemia.
    Pilonetto DV; Pereira NF; Bitencourt MA; Magdalena NI; Vieira ER; Veiga LB; Cavalli IJ; Ribeiro RC; Pasquini R
    Braz J Med Biol Res; 2009 Mar; 42(3):237-43. PubMed ID: 19287902
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.