Variation in the expression of aphidicolin-induced fragile sites in human lymphocyte cultures
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00284909.pdf
Reference19 articles.
1. Brookwell R, Daniel A, Turner G, Fishburn J (1982) The fragile X(q27) form of X-linked mental retardation: FUdR as an inducing agent for fra(X)(q27) expression in lymphocytes, fibroblasts, and amniocytes. Am J Med Genet 13:139?148
2. Daniel A (1986) Clinical implications and classification of the constitutive fragile sites. Am J Med Genet 23:419?427
3. Daniel A, Ekblom L, Phillips S (1984) Constitutive fragile sites 1p31, 3p14, 6q26, and 16q23 and their use as controls for false-negative results with the fragile(X). Am J Med Genet 18:483?491
4. De Braekeleer M, Smith B, Lin CC (1985) Fragile sites and structural rearrangements in cancer. Hum Genet 69:112?116
5. Glover TW, Berger C, Coyle J, Echo B (1984) DNA polymerase a-inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes. Hum Genet 67:136?142
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1. The Role of Fragile Sites in Sporadic Papillary Thyroid Carcinoma;Journal of Thyroid Research;2012
2. Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones;International Journal of Oncology;2010-03-01
3. Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites;BMC Genomics;2009-01-30
4. Novel aphidicolin-inducible common fragile siteFRA9G maps to 9p22.2, within theC9orf39 gene;Genes, Chromosomes and Cancer;2007
5. High-resolution mapping identifies a commonly amplified 11q13.3 region containing multiple genes flanked by segmental duplications;Human Genetics;2006-12-15
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