Xp21.2 contiguous gene syndrome due to deletion involving glycerol kinase and Duchenne muscular dystrophy loci
Justyna Paprocka(Medical University of Silesia), Maciej Adamowicz(Children's Memorial Health Institute), Ewa Popowska(Instytut Matki i Dziecka), Elżbieta Ciara(Children's Memorial Health Institute), Ewa Jamroz(Medical University of Silesia), Justyna Pytel(Medical University of Silesia)
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