Ferguson-Smith, Malcolm A
University of Cambridge
3 papers on CoChatORCID 0000-0001-9372-1381
Most cited papers
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Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome
Borg, I., Freude, K., Kübart, S., Hoffmann, K., Menzel, C., Laccone, F., Firth, H., Ferguson-Smith, M. A., Tommerup, N., Ropers, H.-H., et al. (2005) · European Journal of Human Genetics
Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities
Cited by 95
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The evolution of imprinting: chromosomal mapping of orthologues of mammalian imprinted domains in monotreme and marsupial mammals
Edwards, C. A., Rens, W., Clarke, O., Mungall, A. J., Hore, T., Graves, J. A. M., Dunham, I., Ferguson-Smith, A. C., & Ferguson-Smith, M. A. (2007) · BMC Evolutionary Biology
Genetic Syndromes and ImprintingChromosomal and Genetic Variations
Cited by 44
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Gender verification in sport: the need for change?
Ferguson-Smith, M. A., & Ferris, E. A. (1991) · British Journal of Sports Medicine
Sports, Gender, and SocietySexual Differentiation and Disorders
Cited by 43
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