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Li, L, Moore, P, Ngo, C, Petrovic, V, White, SM, Northrop, E, Ioannou, PA, Gardner, RJM, Slater, HR.
Identification of a haplosufficient 3.6-Mb region in human chromosome 11q14.3→q21.
Cytogenetic and Genome Research
97(3-4)
:
158 -162
2002
view publication
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Daniel, A, Wu, Z, Bennetts, B, Slater, H, Osborn, R, Jackson, J, Pupko, V, Nelson, J, Watson, G, Cooke‐Yarborough, C, et al.
Karyotype, phenotype and parental origin in 19 cases of triploidy.
Prenatal Diagnosis
21(12)
:
1034 -1048
2001
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Apostolopoulos, J, Sparrow, RL, McLeod, JL, Collier, FM, Darcy, PK, Slater, HR, Ngu, C, Gregorio-King, CC, Kirkland, MA.
Identification and Characterization of a Novel Family of Mammalian Ependymin-Related Proteins (MERPs) in Hematopoietic, Nonhematopoietic, and Malignant Tissues.
DNA and Cell Biology
20(10)
:
625 -635
2001
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Voullaire, L, Saffery, R, Earle, E, Irvine, DV, Slater, H, Dale, S, du Sart, D, Fleming, T, Choo, KHA.
Mosaic inv dup(8p) marker chromosome with stable neocentromere suggests neocentromerization is a post‐zygotic event.
American Journal of Medical Genetics
102(1)
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86 -94
2001
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Slater, HR, Ralph, A, Daniel, A, Worthington, S, Roberts, C.
A case of maternal uniparental disomy of chromosome 9 diagnosed prenatally and the related problem of residual trisomy.
Prenatal Diagnosis
20(11)
:
930 -932
2000
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