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Leonard, H, Weaving, L, Eastaugh, P, Smith, L, Delatycki, M, Witt Engerström, I, Christodoulou, J.
Trisomy 21 and Rett syndrome: a double burden..
J Paediatr Child Health
40(7)
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406 -409
2004
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Tumer, Z, Horn, N, Tonnesen, T, Christodoulou, J, Clarke, JTR, Sarkar, B.
Gene symbol: ATP7A. Disease: Menkes disease..
Hum Genet
114(6)
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606
2004
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Rae, C, Joy, P, Harasty, J, Kemp, A, Kuan, S, Christodoulou, J, Cowell, CT, Coltheart, M.
Enlarged temporal lobes in Turner syndrome: an X-chromosome effect?.
Cereb Cortex
14(2)
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156 -164
2004
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Shaw, CJ, Stankiewicz, P, Christodoulou, J, Smith, E, Jones, K, Lupski, JR.
A girl with duplication 17p10-p12 associated with a dicentric chromosome..
Am J Med Genet A
124A(2)
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173 -178
2004
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Colvin, L, Leonard, H, de Klerk, N, Davis, M, Weaving, L, Williamson, S, Christodoulou, J.
Refining the phenotype of common mutations in Rett syndrome..
J Med Genet
41(1)
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25 -30
2004
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