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Cardoso, C, Boys, A, Parrini, E, Mignon-Ravix, C, McMahon, JM, Khantane, S, Bertini, E, Pallesi, E, Missirian, C, Zuffardi, O, et al. Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletionSYMBOL.
Neurology
72(9)
:
784 -792
2008
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Voullaire, L, Wilton, L, Slater, H, Williamson, R. Detection of aneuploidy in single cells using comparative genomic hybridization.
Prenatal Diagnosis
19(9)
:
846 -851
1999
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Slater, H, Shaw, JH, Dawson, G, Bankier, A, Forrest, SM. Maternal uniparental disomy of chromosome 13 in a phenotypically normal child..
Journal of Medical Genetics
31(8)
:
644
1994
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Slater, HR, Tiong, T, Konstantakopoulos, S, Sham, C, Petrovic, V, Voullaire, L, Kannourakis, G. Cytogenetic and DNA analysis of two neuroectodermal tumors without a simple t(11;22).
Cancer Genetics
83(1)
:
12 -17
1995
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Chia, NL, Slater, HR, Potter, JM. Detection of segmental chromosome copy number gains by improved fluorescence in situ hybridization techniques..
Journal of the Association of Genetic Technologists
41(1)
:
5 -11
2015
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