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 *

122 related articles for article (PubMed ID: 2017342)

  • 21. VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies?
    Porteous ME; Cross I; Burn J
    Am J Med Genet; 1992 Aug; 43(6):1032-4. PubMed ID: 1415330
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Retinoblastoma in association with the chromosome breakage syndromes Fanconi's anaemia and Bloom's syndrome: clinical and cytogenetic findings.
    Gibbons B; Scott D; Hungerford JL; Cheung KL; Harrison C; Attard-Montalto S; Evans M; Birch JM; Kingston JE
    Clin Genet; 1995 Jun; 47(6):311-7. PubMed ID: 7554365
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Fibroblasts from patients with Fanconi's anemia are not deficient in excision of thymine dimer.
    Klocker H; Burtscher HJ; Auer B; Hirsch-Kauffmann M; Schweiger M
    Eur J Cell Biol; 1985 May; 37():240-2. PubMed ID: 4029168
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Chromosomal breaks in T and B lymphocytes in Fanconi's anemia.
    Bushkell LL; Kersey JH; Cervenka J
    Clin Genet; 1976 Jun; 9(6):583-7. PubMed ID: 1084238
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Relationship of spontaneous chromosome instability and sister chromatid exchanges in Fanconi's anemia].
    Nazarenko SA; Burmakina IuE
    Biull Eksp Biol Med; 1984 Sep; 98(9):334-6. PubMed ID: 6487791
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. [What do the chromosome-breakage syndromes teach us about the care of persons at increased risk for malignant diseases?].
    German J
    Cas Lek Cesk; 1986 Jul; 125(30):921-6. PubMed ID: 3731231
    [No Abstract]   [Full Text] [Related]  

  • 28. Carcinogen-induced chromosome breakage in Fanconi's anaemia heterozygous cells.
    Auerbach AD; Wolman SR
    Nature; 1978 Jan; 271(5640):69-71. PubMed ID: 625326
    [No Abstract]   [Full Text] [Related]  

  • 29. Fanconi anemia. Chromosome breakage and cell cycle studies.
    Berger R; Le Coniat M; Gendron MC
    Cancer Genet Cytogenet; 1993 Aug; 69(1):13-6. PubMed ID: 8374893
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Fanconi's anemia].
    Chueca C; Herrer A; Pueyo C
    Aten Primaria; 1993 Mar; 11(5):261-2. PubMed ID: 8471713
    [No Abstract]   [Full Text] [Related]  

  • 31. Differentiation of Nijmegen breakage syndrome from Fanconi anemia.
    Rao VB; Kerketta L; Korgaonkar S; Ghosh K
    Genet Mol Res; 2007 Sep; 6(3):622-6. PubMed ID: 18050081
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Differentiation of Fanconi anemia from idiopathic aplastic anemia by induced chromosomal breakage study using mitomycin-C (MMC).
    Talwar R; Choudhry VP; Kucheria K
    Indian Pediatr; 2004 May; 41(5):473-7. PubMed ID: 15181297
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Synergism of bromodeoxyuridine and mitomycin C in the production of chromosomal aberrations in Fanconi's anemia].
    Frías S; Molina B; Carnevale A
    Rev Invest Clin; 1989; 41(1):31-5. PubMed ID: 2499026
    [TBL] [Abstract][Full Text] [Related]  

  • 34. G2 chromosomal radiosensitivity in Fanconi's anemia.
    Bigelow SB; Rary JM; Bender MA
    Mutat Res; 1979 Nov; 63(1):189-99. PubMed ID: 522866
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Recent advances in chromosome breakage syndromes and their diagnosis.
    Mathur R; Chowdhury MR; Singh G
    Indian Pediatr; 2000 Jun; 37(6):615-25. PubMed ID: 10869141
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatal diagnosis of Fanconi anemia.
    Voss R; Kohn G; Shaham M; Benzur Z; Arnon J; Ornoy A; Yaffe H; Golbus M; Auerbach AD
    Clin Genet; 1981 Sep; 20(3):185-90. PubMed ID: 7307316
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Premature centromere division: a possible manifestation of chromosome instability.
    Méhes K; Bühler EM
    Am J Med Genet; 1995 Mar; 56(1):76-9. PubMed ID: 7747791
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Is mitomycin C-induced chromosome breakage always required for the diagnosis of Fanconi aplastic anemia?
    Ozsoylu S
    Pediatr Hematol Oncol; 1999; 16(3):271, 273. PubMed ID: 10326228
    [No Abstract]   [Full Text] [Related]  

  • 40. Fanconi's anemia. Clinical study of six cases.
    Gastearena J; Giralt M; Orue MT; Oyarzabal FJ; Perez-Equiza E; Uriz MJ
    Am J Pediatr Hematol Oncol; 1986; 8(3):173-7. PubMed ID: 3766907
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.