DOI:
10.1055/s-00034916
Nervenheilkunde
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References
Stuhrmann M. et al.
Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenita.
Hum Genet 1991;
86: 414-5.
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