Details
Role
Clinical Geneticist
Group
Clinical Services
Top Publications
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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)
:
103 -114
2003
view publication
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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)
:
120
2003
view publication
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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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946 -955
2003
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Savarirayan, R, White, SM, Goodman, FR, Graham, JM, Delatycki, MB, Lachman, RS, Rimoin, DL, Everman, DB, Warman, ML.
Broad phenotypic spectrum caused by an identical heterozygous CDMP‐1 mutation in three unrelated families.
American Journal of Medical Genetics Part A
117A(2)
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136 -142
2003
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Tassicker, R, Savulescu, J, Skene, L, Marshall, P, Fitzgerald, L, Delatycki, MB.
Prenatal diagnosis requests for Huntington's disease when the father is at risk and does not want to know his genetic status: clinical, legal, and ethical viewpoints.
The BMJ
326(7384)
:
331
2003
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