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A pattern of inheritance in which mutation in only one copy of a gene is sufficient to cause an effect, for example the gene that causes Huntington's disease.

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Newborn screening: the UK National Screening Committee answers your questions 29 November 2021 Comment
The making of an Olympic athlete 25 July 2016 Comment
Policing preimplantation genetic diagnosis: patients first please 18 February 2013 Comment
'Marry out?' Some surprising consequences of genetic disease risk among Ashkenazi Jews 28 May 2012 Comment

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