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Results: 3

Authors: Runte, M Farber, C Lich, C Zeschnigk, M Buchholz, T Smith, A Van Maldergem, L Burger, J Muscatelli, F Gillessen-Kaesbach, G Horsthemke, B Buiting, K
Citation: M. Runte et al., Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15, EUR J HUM G, 9(7), 2001, pp. 519-526

Authors: Muscatelli, F Abrous, DN Massacrier, A Boccaccio, I La Moal, M Cau, P Cremer, H
Citation: F. Muscatelli et al., Disruption of the mouse Necdin gene results in hypothalamic and behavioralalterations reminiscent of the human Prader-Willi syndrome, HUM MOL GEN, 9(20), 2000, pp. 3101-3110

Authors: Boccaccio, I Glatt-Deeley, H Watrin, F Roeckel, N Lalande, M Muscatelli, F
Citation: I. Boccaccio et al., The human MAGEL2 gene and its mouse homologue are paternally expressed andmapped to the Prader-Willi region, HUM MOL GEN, 8(13), 1999, pp. 2497-2505
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