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2. Familial X-linked retardation representing a severe multihandicap syndrome with an X chromosome abnormality;Harvey, J.; Judge, C.; Wiener, S.;J Med Genet; 14: with decreasing mobility, scoliosis, and the 46-50,1977
3. Fragile sites on human chromosomes: development of paraplegic or tetraplegic signs. demonstration of their dependence on the type of tissue Familial recurrence of Rett's syndrome is infreculture medium;Sutherland, G.R.;Science,1977
4. X-linked mental retardation and the fragile X quently reported,28 29 and low recurrence risks syndrome: a clinical approach;Fryns, J.P.,1989
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