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van de Sluis, B
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Citation: Jhp. Hackstein et al., Towards an understanding of the genetics of human male infertility: lessons from flies, TRENDS GEN, 16(12), 2000, pp. 565-572
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Citation: Fj. Hes et al., Cryptic von Hippel-Lindau disease: germline mutations in patients with haemangioblastoma only, J MED GENET, 37(12), 2000, pp. 939-943
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van Tilburg, JHO
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Citation: Jho. Van Tilburg et al., The exon 16-3t variant of the sulphonylurea receptor gene is not a risk factor for Type II diabetes mellitus in the Dutch Breda cohort, DIABETOLOG, 43(5), 2000, pp. 681-682
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van de Sluis, BJA
Breen, M
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van Wolferen, M
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Rothuizen, J
Cox, DW
Wijmenga, C
van Oost, BA
Citation: Bja. Van De Sluis et al., Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16, HUM MOL GEN, 8(3), 1999, pp. 501-507
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Giltay, JC
Kastrop, PMM
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Citation: Jc. Giltay et al., Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISH, CYTOG C GEN, 84(1-2), 1999, pp. 67-72
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Citation: Jmjc. Scheres et al., Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas - Possible trisomic or tetrasomic zygote rescue in fetal teratoma with anadditional isochromosome 1q, CANC GENET, 115(1), 1999, pp. 1-10
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Kuipers, J
Vaandrager, JW
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Pearson, PL
Scheres, J
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Bast, BJEG
Citation: J. Kuipers et al., Fluorescence in situ hybridization analysis shows the frequent occurrence of 14q32.3 rearrangements with involvement of immunoglobulin switch regionsin myeloma cell lines, CANC GENET, 109(2), 1999, pp. 99-107
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