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See Latest ArticlesMultilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci
Human Molecular Genetics, 11/25/09
Azzi S et al. – The results show for the first time that multilocus LOM can also concern RSS patients. Moreover, LOM can involve both paternally and maternally methylated loci in the same patient.
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HO-1 polymorphism as a genetic determinant behind the malaria resistance afforded by haemolytic disorders
Medical Hypotheses, 02/09/10
Potocki-Shaffer syndrome: Comprehensive clinical assessment, review of the literature, and proposals for medical management
American Journal of Medical Genetics, 02/09/10
FOXE3 plays a significant role in autosomal recessive microphthalmia
American Journal of Medical Genetics, 02/09/10
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