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Medical condition
Ring chromosome 18
Other names
Ring chromosome 18[1]
Child with ring chromosome 18
Specialty
Medical genetics
Ring chromosome 18 is a genetic condition caused by a deletion of the two ends of chromosome 18 followed by the formation of a ring-shaped chromosome. It was first reported in 1964.[2]
^RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Ring chromosome 18 syndrome". www.orpha.net. Retrieved 16 August 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)
^Gropp et al (1964). Multiple congenital anomalies associated with a partially ring-shaped chromosome probably derived from chromosome no. 18 in man. Nature 202:829-30.
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