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Results: 1-3 |
Results: 3
Chromosome 15 uniparental disomy is not frequent in Angelman syndrome.
Authors: Knoll, J. H. M. Glatt, K.A. Nicholls, R. D. Malcolm, S. Lalande, M.
Citation: M. Knoll, J. H. et al., Chromosome 15 uniparental disomy is not frequent in Angelman syndrome., American journal of human genetics , 48-I(1), 1991, pp. 16-21
Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers.
Authors: Knoll, J. H. M. Nicholls, R. D. Magenis, R.E. Glatt,K. Graham,J.M. Kaplan, L. Lalande, M.
Citation: M. Knoll, J. H. et al., Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers., American journal of human genetics , 47-I(1), 1990, pp. 149-155
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. i. cases due to deletions involving chromosome band 16p13.3
Authors: Wilkie, A. O. M. Buckle, V. I. Harris, P. C. Lamb, J. Barton, N. J. Reeders, S. T. Lindenbaum, R H. Nicholls, R. D. Barrow, M. Bethlenfalvay, N. C. Hutz, M. H. Tolmie, J. L. Weatherall, D. J. Higgs, D. R.
Citation: M. Wilkie, A. O. et al., Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. i. cases due to deletions involving chromosome band 16p13.3, American journal of human genetics , 46-II(6), 1990, pp. 1112-1126
Risultati: 1-3 |