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Citation: Aa. Geldof et al., Clonally related but phenotypically divergent human cancer cell lines derived from a single follicular thyroid cancer recurrence (TT2609), THYROID, 11(10), 2001, pp. 909-917
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Citation: Hj. Van De Vrugt et al., Cloning and characterization of murine Fanconi anemia group A gene: Fanca protein is expressed in lymphoid tissues, testis, and ovary, MAMM GENOME, 11(4), 2000, pp. 326-331
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Citation: Jp. De Winter et al., Isolation of a cDNA representing the Fanconi anemia complementation group E gene, AM J HU GEN, 67(5), 2000, pp. 1306-1308
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Citation: J. Cloos et al., Inherited susceptibility to bleomycin-induced chromatid breaks in culturedperipheral blood lymphocytes, J NAT CANC, 91(13), 1999, pp. 1125-1130
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Citation: Q. Waisfisz et al., Spontaneous functional correction of homozygous Fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism, NAT GENET, 22(4), 1999, pp. 379-383
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Citation: M. Wijker et al., Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene, EUR J HUM G, 7(1), 1999, pp. 52-59
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Citation: Jsp. Van Den Berg et al., Type III collagen deficiency in saccular intracranial aneurysms - Defect in gene regulation?, STROKE, 30(8), 1999, pp. 1628-1631
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Citation: Q. Waisfisz et al., A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCA, P NAS US, 96(18), 1999, pp. 10320-10325
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Citation: Q. Waisfisz et al., The Fanconi anemia group E gene, FANCE, maps to chromosome 6p, AM J HU GEN, 64(5), 1999, pp. 1400-1405