Authors:
Khalifa, MM
Struthers, JL
Maurice, S
Harrison, K
Duncan, AMV
Citation: Mm. Khalifa et al., Methylation of HpaII site at the human DXS16 locus on Xp22 as an assay forabnormal patterns of X inactivation, AM J MED G, 98(1), 2001, pp. 64-69
Citation: Jp. Rossiter et al., Diencephalic neuronal hamartoma associated with congenital obstructive hydrocephalus, anophthalmia, cleft lip and palate and severe mental retardation: a possible new syndrome, ACT NEUROP, 99(6), 2000, pp. 685-690
Citation: Jl. Struthers et al., Parental origin of the isochromosome 12p in Pallister-Killian syndrome: Molecular analysis of one patient and review of the reported cases, AM J MED G, 84(2), 1999, pp. 111-115