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de Silva, MG, Elliott, K, Dahl, H-H, Fitzpatrick, E, Wilcox, S, Delatycki, M, Williamson, R, Efron, D, Lynch, M, Forrest, S.
Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype.
Journal of Medical Genetics
40(10)
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733
2003
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Delatycki, MB, Danks, A, Churchyard, A, Zhou, X-P, Eng, C.
De novo germline PTEN mutation in a man with Lhermitte-Duclos disease which arose on the paternal chromosome and was transmitted to his child with polydactyly and Wormian bones.
Journal of Medical Genetics
40(8)
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e92
2003
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Weaving, LS, Williamson, SL, Bennetts, B, Davis, M, Ellaway, CJ, Leonard, H, Thong, M, Delatycki, M, Thompson, EM, Laing, N, et al.
Effects of MECP2 mutation type, location and X‐inactivation in modulating Rett syndrome phenotype.
American Journal of Medical Genetics Part A
118A(2)
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103 -114
2003
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Delatycki, MB.
Commentary on Spriggs: genetically selected baby free of inherited predisposition to early onset Alzheimer’s disease.
Journal of Medical Ethics
29(2)
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120
2003
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Squitieri, F, Gellera, C, Cannella, M, Mariotti, C, Cislaghi, G, Rubinsztein, DC, Almqvist, EW, Turner, D, Bachoud‐Lévi, A, Simpson, SA, et al.
Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course.
Brain
126(4)
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2003
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