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Clinical Genetics|November 1, 1988
Complex chromosome rearrangements involving chromosomes 1;3 and 2;3 in two abnormal childrenL E Voullaire, G C WebbJournal of Medical Genetics|July 1, 1989
Fragile X testing in a diagnostic cytogenetics laboratoryL E Voullaire, G C Webb, M LevershaHuman 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 RogersAmerican 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.Journal of Paediatrics and Child Health|February 1, 1990
Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p11.2 p11.2) (Smith-Magenis syndrome)A F Colley, M A Leversha, L E Voullaire, et al.Cytogenetics and Cell Genetics|January 1, 1992
Absence of satellite III DNA in the centromere and the proximal long-arm region of human chromosome 14: analysis of a 14p- variantE Earle, L E Voullaire, L Hills, et al.American Journal of Medical Genetics|June 1, 1993
Confirmation of trisomy 22 in two cases using chromosome painting: comparison with t(11;22)H R Slater, L E Voullaire, C E Vaux, 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.Pageof 2