All Stories

  1. Phosphorylation of pRb: mechanism for RB pathway inactivation inMYCN-amplified retinoblastoma
  2. Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2 (UCP2)
  3. Prenatal diagnosis in haemophilia A: experience of the genetic diagnostic laboratory
  4. Severe and moderate haemophilia A and B in US females
  5. Genotype and Phenotype Correlations in 417 Children With Congenital Hyperinsulinism