DOI:
10.1055/s-00000034
Klinische Pädiatrie
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References
Schwartzman JS, Bernardino A, Nishimura A, Gomes RR, Zatz M.
Rett sindrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 gene.
Neuropediatrics 2001; 32: 162-164
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