| Literature DB >> 527247 |
Abstract
A 12-year-old by with unusual face and hearing loss was diagnosed as having frontometaphyseal dysplasia. He also had congenital urinary tract malformations and chronic urinary tract infection. The cranial and facial bones of the patient were studied by roentgen cephalometric analysis.Entities:
Mesh：
Year: 1979 PMID： 527247 DOI： 10.1111/j.1399-0004.1979.tb01348.x
Source DB: PubMed Journal: Clin Genet ISSN： 0009-9163 Impact factor: 4.438