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Citation: L. Ries et al., Prenatal diagnosis of a novel COL1A1 mutation in osteogenesis imperfecta type I carried through full term pregnancy, PRENAT DIAG, 20(11), 2000, pp. 876-880
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Citation: E. Pras et al., A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family, INV OPHTH V, 41(11), 2000, pp. 3511-3515
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Citation: D. Gothelf et al., Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome, SCHIZOPHR R, 35(2), 1999, pp. 105-112
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Citation: A. Kauschansky et al., D-penicillamine-induced pancreatic islet autoantibody production is independent of the immunogenetic background: A lesson from patients with Wilson'sdisease, CLIN IMM IM, 89(3), 1998, pp. 279-283
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Citation: I. Mcintosh et al., Mutation analysis of LMX1B gene in nail-patella syndrome patients, AM J HU GEN, 63(6), 1998, pp. 1651-1658