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Journal of Medical Genetics|July 1, 1989
Fragile X testing in a diagnostic cytogenetics laboratoryL E Voullaire, G C Webb, M LevershaClinical Genetics|November 1, 1988
Complex chromosome rearrangements involving chromosomes 1;3 and 2;3 in two abnormal childrenL E Voullaire, G C WebbHuman Genetics|June 1, 1987
Chromosome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23L E Voullaire, G C Webb, M A LevershaAmerican Journal of Medical Genetics|August 1, 1988
Duplication of a small segment of 5p due to maternal recombination within a paracentric shiftG C Webb, L E Voullaire, J G RogersHuman Genetics|June 1, 1991
The importance of further cytogenetic and molecular investigation of acrocentric variants: justification by presentation of a case [t(8;14)(q24;p11)]L Hills, E Earle, M Wilson, et al.Human Genetics|April 1, 1989
Non C-banding variants in some normal families might be homogeneously staining regionsG C Webb, E J Krumins, S Z Eichenbaum, et al.Journal of Medical Genetics|February 1, 1982
Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardationG C Webb, J L Halliday, D B Pitt, et al.American Journal of Medical Genetics|June 1, 1991
Two forms of ring 13 in a child with rhabdomyosarcomaL E Voullaire, V Petrovic, L J Sheffield, et al.American Journal of Human Genetics|June 1, 1993
A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein: activation of a latent centromere?L E Voullaire, H R Slater, V Petrovic, et al.The New Zealand Medical Journal|October 27, 1995
Alcohol and pregnancy: doctors' attitudes, knowledge and clinical practiceA M Leversha, R E MarksPageof 10