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Raskind, W H; Niakan, K K; Wolff, J et al. (2000) Mapping of a syndrome of X-linked thrombocytopenia with Thalassemia to band Xp11-12: further evidence of genetic heterogeneity of X-linked thrombocytopenia. Blood 95:2262-8
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Raskind, W H; Bolin, T; Wolff, J et al. (1998) Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34. Hum Genet 102:93-7
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Chansky, H; Robbins, J R; Cha, S et al. (1998) Expression of cartilage extracellular matrix and potential regulatory genes in a new human chondrosarcoma cell line. J Orthop Res 16:521-30
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Raskind, W H; Conrad 3rd, E U; Matsushita, M et al. (1998) Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses. Hum Mutat 11:231-9
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Raskind, W H; Steinmann, L; Najfeld, V (1998) Clonal development of myeloproliferative disorders: clues to hematopoietic differentiation and multistep pathogenesis of cancer. Leukemia 12:108-16
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Higano, C S; Chielens, D; Raskind, W et al. (1997) Use of alpha-2a-interferon to treat cytogenetic relapse of chronic myeloid leukemia after marrow transplantation. Blood 90:2549-54
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Horwitz, M; Benson, K F; Li, F Q et al. (1997) Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2. Am J Hum Genet 61:873-81
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Raskind, W H; Pericak-Vance, M A; Lennon, F et al. (1997) Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2. Am J Med Genet 74:26-36
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Raskind, W H; Conrad, E U; Matsushita, M (1996) Frequent loss of heterozygosity for markers on chromosome arm 10q in chondrosarcomas. Genes Chromosomes Cancer 16:138-43
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Raskind, W H; Conrad, E U; Chansky, H et al. (1995) Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11. Am J Hum Genet 56:1132-9
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