| 1 | FRA11B, DEL11QD
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| Co-localisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome: evidence for a common mechanism of chromosome breakage.
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| Jones C, Mullenbach R, Grossfeld P, Auer R, Favier R, Chien K, James M, Tunnacliffe A, Cotter F.
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| Hum Mol Genet 9(8):1201-8. 2000
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| 2 | DEL11QD, CBL, FRA11B
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| Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2.
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| Jones C, et al.
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| Nature 376 : 145-149. 1995
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| 3 | FRA11B, CBL, DEL11QD
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| Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3.
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| Jones C, et al.
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| Hum Mol Genet 3 : 2123-2130. 1994
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| 4 | FRA11B
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| Chromosome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23.
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| Voullaire LE, Webb GC, Leversha MA.
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| Hum Genet 76 : 202-204. 1987
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| 5 | FHIT, FRA10A, FRA11A, FRA11B, FRA12A, FRA7A
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| Report of the committee on chomosome rearrangements in neoplasia and on fragile sites.
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| de La Chapelle A, et al.
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| (HGM7) Cytogenet Cell Genet 37 : 274-311. 1984
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| 6 | FRA6A, FRA11B, FRA9A, FRA9B
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| Heritable fragile sites on human chromosomes. X. New folate-sensitivefragile sites: 6p23, 9p21, 9q32, 11q23.
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| Sutherland GR, et al.
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| Am J Hum Genet 35 : 432-437. 1983
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