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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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Ling, L, Swain, M, Conyers, R, Bruno, D, Whitlam, J, Slater, H.
A powerful new approach to measuring engraftment using copy number variations and droplet digital PCR, exemplified in a complex allogeneic bone marrow transplantation case.
Pathology
47:
s87
2015
view publication
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Bruno, DL, Ganesamoorthy, D, Thorne, NP, Ling, L, Bahlo, M, Forrest, S, Veenendaal, M, Katerelos, M, Skene, A, Ierino, FL, et al.
Use of Copy Number Deletion Polymorphisms to Assess DNA Chimerism.
Clinical Chemistry
60(8)
:
1105 -1114
2014
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Inaba, Y, Schwartz, CE, Bui, QM, Li, X, Skinner, C, Field, M, Wotton, T, Hagerman, RJ, Francis, D, Amor, DJ, et al.
Early Detection of Fragile X Syndrome: Applications of a Novel Approach for Improved Quantitative Methylation Analysis in Venous Blood and Newborn Blood Spots.
Clinical Chemistry
60(7)
:
963 -973
2014
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Godler, DE, Amor, DJ, Slater, HR.
Methylation Analysis in Newborn Screening for Fragile X Syndrome.
JAMA Neurology
71(6)
:
800 -800
2014
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