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Schwartzman J.S., Bernardino A., Nishimura A., Gomes R.R., Zatz M. Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 gene.// Neuropediatrics. 2001.32. P.162-164.
Schwartzman J.S., Bernardino A., Nishimura A., Gomes R.R., Zatz M. Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 gene.// Neuropediatrics. 2001.32. P.162-164.
