Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 gene. (Q34088108)
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Current Data About Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 gene.
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(P1476) "Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 gene" (language: en)
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(P2093) Schwartzman JS
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Bernardino A
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Gomes RR
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Zatz M
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External Links
(P356) 10.1055/S-2001-16620
(P698) 11521215