Nielsen J.B., Henriksen K.F. 2001a
Nielsen J.B., Henriksen K.F., Hansen C, Silahtaroglu A., Schwartz M., Tommerup N. MECP2 mutations in Danish patients with Rett syndrome: high frequency of mutations but no consistent correlations with clinical severity or with the X chromosome inactivation pattern.//Eur. J.Hum.Genet. 2001a.9. P.178-184.
