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Results: 1-6 |
Results: 6

Authors: RODENHISER D OMALLEY FP MANCINI D AINSWORTH P SINGH S CHAKRABORTY P KERKVLIET N
Citation: D. Rodenhiser et al., EVALUATING DNA METHYLATION PATTERNS AT MUTATIONAL HOTSPOTS USING ARCHIVAL TISSUES, Laboratory investigation, 76(1), 1997, pp. 1080-1080

Authors: MANCINI D SINGH S AINSWORTH P RODENHISER D
Citation: D. Mancini et al., CONSTITUTIVELY METHYLATED CPG DINUCLEOTIDES AS MUTATION HOT-SPOTS IN THE RETINOBLASTOMA GENE (RB1), American journal of human genetics, 61(1), 1997, pp. 80-87

Authors: RODENHISER D CHAKRABORTY P ANDREWS J AINSWORTH P MANCINI D LOPES E SINGH S
Citation: D. Rodenhiser et al., HETEROGENEOUS POINT MUTATIONS IN THE BRCA1 BREAST-CANCER SUSCEPTIBILITY GENE OCCUR IN HIGH-FREQUENCY AT THE SITE OF HOMONUCLEOTIDE TRACTS, SHORT REPEATS AND METHYLATABLE CPG CPNPG MOTIFS/, Oncogene, 12(12), 1996, pp. 2623-2629

Authors: RODENHISER D HOVLAND K
Citation: D. Rodenhiser et K. Hovland, A NOVEL RSAI POLYMORPHISM WITHIN INTRON-39 OF THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE, Human genetics, 95(2), 1995, pp. 241-242

Authors: AINSWORTH P RODENHISER D STUART A JUNG J
Citation: P. Ainsworth et al., CHARACTERIZATION OF AN INTRON-31 SPLICE JUNCTION MUTATION IN THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE, Human molecular genetics, 3(7), 1994, pp. 1179-1181

Authors: COSTA T MACKENZIE J RODENHISER D AINSWORTH P
Citation: T. Costa et al., WATSON SYNDROME-ASSOCIATED WITH A DELETION AT THE NF1 LOCUS, American journal of human genetics, 53(3), 1993, pp. 419-419
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