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Results: 1-4 |
Results: 4
DETECTION OF CMT1A DUPLICATION AND HNPP DELETIONS WITH REDUCED DEPENDENCE ON DOSAGE ANALYSIS
Authors: HARVEY J HACKWELL S STEVENS C BULLMAN H
Citation: J. Harvey et al., DETECTION OF CMT1A DUPLICATION AND HNPP DELETIONS WITH REDUCED DEPENDENCE ON DOSAGE ANALYSIS, Journal of Medical Genetics, 34, 1997, pp. 1411-1411
HEREDITARY DESMOID DISEASE DUE TO A FRAMESHIFT MUTATION AT CODON-1924OF THE APC GENE
Authors: ECCLES DM VANDERLUIJT R BREUKEL C BULLMAN H BUNYAN D FISHER A BARBER J DUBOULAY C PRIMROSE J BURN J FODDE R
Citation: Dm. Eccles et al., HEREDITARY DESMOID DISEASE DUE TO A FRAMESHIFT MUTATION AT CODON-1924OF THE APC GENE, American journal of human genetics, 59(6), 1996, pp. 1193-1201
INSERT SIZE AND FLANKING HAPLOTYPE IN FRAGILE-X AND NORMAL-POPULATIONS - POSSIBLE MULTIPLE ORIGINS FOR THE FRAGILE-X MUTATION
Authors: MACPHERSON JN BULLMAN H YOUINGS SA JACOBS PA
Citation: Jn. Macpherson et al., INSERT SIZE AND FLANKING HAPLOTYPE IN FRAGILE-X AND NORMAL-POPULATIONS - POSSIBLE MULTIPLE ORIGINS FOR THE FRAGILE-X MUTATION, Human molecular genetics, 3(3), 1994, pp. 399-405
POPULATION STUDIES OF THE FRAGILE-X - A MOLECULAR APPROACH
Authors: JACOBS PA BULLMAN H MACPHERSON J YOUINGS S ROONEY V WATSON A DENNIS NR
Citation: Pa. Jacobs et al., POPULATION STUDIES OF THE FRAGILE-X - A MOLECULAR APPROACH, Journal of Medical Genetics, 30(6), 1993, pp. 454-459
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