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Citation: R. Sood et al., Cloning and characterization of 13 novel transcripts and the human RC58 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus, GENOMICS, 73(2), 2001, pp. 211-222
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Citation: Mh. Lee et al., Fine-mapping, mutation analyses, and structural mapping of cerebrotendinous xanthomatosis in US pedigrees, J LIPID RES, 42(2), 2001, pp. 159-169
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Citation: Jf. Xu et al., Linkage and association studies of prostate cancer susceptibility: Evidence for linkage at 8p22-23, AM J HU GEN, 69(2), 2001, pp. 341-350
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Citation: Jf. Xu et al., Evaluation of linkage and association of HPC2/ELAC2 in patients with familial or sporadic prostate cancer, AM J HU GEN, 68(4), 2001, pp. 901-911
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Citation: R. Sood et al., The human RGL (RalGDS-like) gene: cloning, expression analysis and genomicorganization, BBA-GENE ST, 1491(1-3), 2000, pp. 285-288
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Citation: R. Berry et al., Linkage analyses at the chromosome 1 Loci 1q24-25 (HPC1), 1q42.2-43 (PCAP), and 1p36 (CAPB) in families with hereditary prostate cancer, AM J HU GEN, 66(2), 2000, pp. 539-546
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Citation: J. Marcelino et al., CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome, NAT GENET, 23(3), 1999, pp. 319-322