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Xp21.2 contiguous gene syndrome due to deletion involving glycerol kinase and Duchenne muscular dystrophy loci

Jamroz Ewa, Paprocka Justyna, Popowska Ewa, Pytel Justyna, Ciara Elzbieta, Adamowicz Maciej

Year : 2010| Volume: 58| Issue : 4 | Page no: 670-671

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1 A female patient with Xp21 gene deletion syndrome
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