PubMed · 942238
D13 ring chromosome syndrome.
Abstract
A case of ring D13 chromosome, confirmed by trypsin banding, is described. Reviewing 21 cases from published reports, the most common features of this syndrome are microcephaly and associated mental retardation, poor uterine growth, deformed auricles, hypertelorism, epicanthus, broad nasal bridge, and genital defects in males.
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
A Mccandless, S Walker. 1976. D13 ring chromosome syndrome.. https://doi.org/10.1136/adc.51.6.449
Cite the original work for its findings. Save a collection to share your selection of sources.