Fallbericht
Neurocognitive Functioning in a Young Female with Weaver Syndrome
Research Article
Association Study of IVS8TGmTn Polymorphism and Cystic Fibrosis Disease in a Tunisian Population
Identification of a Novel Mutation in the Human ARSB Gene on Chromosome 5q14.1 for Autosomal Recessive Mucopolysaccharidosis Type VI Patients in Southwest Colombia
PROK2 and PNCK – Novel Proteins Present in Follicular Fluid of Mature and Immature Human Oocytes: Preliminary Study
Biotinidase Deficiency Presenting as Hyperventilation Syndrome