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