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American Journal of Human Genetics|January 1, 1996
Lack of X inactivation associated with maternal X isodisomy: evidence for a counting mechanism prior to X inactivation during human embryogenesisB R Migeon, P Jeppesen, B S Torchia, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Direct microdissection and microcloning of a translocation breakpoint region, t(1;11)(q42.2;q21), associated with schizophreniaW J Muir, C M Gosden, A J Brookes, et al.
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