Definition: Monosomy is the state of having a single copy of a chromosome pair instead of the usual two copies found in diploid cells. Monosomy can be partial if a portion of the second chromosome copy is present. Monosomy, or partial monosomy, is the cause of some human diseases such as Turner syndrome and Cri du Chat syndrome.
Source: National Human Genome Research Institute's Talking Glossary of Genetic Terms
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Monosomy
Source: National Human Genome Research Institute's Talking Glossary of Genetic Terms