| Literature DB >> 3783629 |
Abstract
A de novo chromosome abnormality interpreted as a terminal deletion of chromosome 10, del(10)(pter----q25.2:), was ascertained in a newborn female with multiple malformations. The clinical features observed at birth and on follow up at 10 months of age are described and compared with previously reported cases.Entities:
Mesh:
Year: 1986 PMID: 3783629 PMCID: PMC1049791 DOI: 10.1136/jmg.23.5.478
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318