Monosomy 10qter: a new case.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 1583662.
- Also identified by PMC identifier 1015956.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
A new case of terminal deletion 10q26-qter is described. The phenotypic features are compatible with those of the previously reported cases. Deafness is reported for the first time.
Medical subject headings
- Abnormalities, Multiple
- Aneuploidy
- Chromosomes, Human, Pair 10