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Tan, TY, Bankier, A, Slater, HR, Northrop, EL, Zacharin, M, Savarirayan, R.
A patient with monosomy 1p36, atypical features and phenotypic similarities with Cantu syndrome.
American Journal of Medical Genetics Part A
139A(3)
:
216 -220
2005
view publication
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Schüle, B, Albalwi, M, Northrop, E, Francis, DI, Rowell, M, Slater, HR, Gardner, RM, Francke, U.
Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome.
BMC Medical Genomics
6(1)
:
18
2005
view publication
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Northrop, EL, Ren, H, Bruno, DL, McGhie, JDR, Coffa, J, Schouten, J, Choo, KHA, Slater, HR.
Detection of cryptic subtelomeric chromosome abnormalities and identification of anonymous chromatin using a quantitative multiplex ligation‐dependent probe amplification (MLPA) assay.
Human Mutation
26(5)
:
477 -486
2005
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Slater, HR, Bailey, DK, Ren, H, Cao, M, Bell, K, Nasioulas, S, Henke, R, Choo, KHA, Kennedy, GC.
High-Resolution Identification of Chromosomal Abnormalities Using Oligonucleotide Arrays Containing 116,204 SNPs.
American Journal of Human Genetics
77(5)
:
709 -726
2005
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Loesch, DZ, Bui, QM, Kelso, W, Huggins, RM, Slater, H, Warne, G, Bergman, P, Rodda, C, Mitchell, RJ, Prior, M.
Effect of Turner's syndrome and X-linked imprinting on cognitive status: analysis based on pedigree data.
Brain and Development
27(7)
:
494 -503
2005
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