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Citation: D. Tentler et al., A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome, J MED GENET, 37(2), 2000, pp. 128-131
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Citation: T. Carling et al., Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor, J CLIN END, 85(5), 2000, pp. 2042-2047
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Citation: P. Gustavsson et al., Occupational exposure and lung cancer risk: A population-based case-referent study in Sweden, AM J EPIDEM, 152(1), 2000, pp. 32-40
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Citation: N. Draptchinskaia et al., The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia, NAT GENET, 21(2), 1999, pp. 169-175
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Citation: D. Tentler et al., Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia, EUR J HUM G, 7(5), 1999, pp. 541-548
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Citation: P. Gustavsson et al., Mortality and cancer incidence among laboratory technicians in medical research and routine laboratories (Sweden), CANC CAUSE, 10(1), 1999, pp. 59-64
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Citation: H. Matsson et al., Truncating ribosomal protein S19 mutations and variable clinical expression in Diamond-Blackfan anemia, HUM GENET, 105(5), 1999, pp. 496-500
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Citation: P. Gustavsson et al., Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3), AM J MED G, 82(4), 1999, pp. 348-351
Citation: M. Pollan et P. Gustavsson, High-risk occupations for breast cancer in the Swedish female working population, AM J PUB HE, 89(6), 1999, pp. 875-881
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Citation: H. Cario et al., A microdeletion syndrome due to a 3-Mb deletion on 19q13.2 - Diamond-Blackfan anemia associated with macrocephaly, hypotonia, and psychomotor retardation, CLIN GENET, 55(6), 1999, pp. 487-492
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Citation: U. Ramenghi et al., Diamond-Blackfan anaemia in the Italian population, BR J HAEM, 104(4), 1999, pp. 841-848