A computerised data base for the diagnosis of rare dysmorphic syndromes.
Open Access
- 1 April 1984
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 21 (2), 121-123
- https://doi.org/10.1136/jmg.21.2.121
Abstract
A system is described for the computerised storage and retrieval of information on rare dysmorphic syndromes. The clinician can ask a microcomputer for a list of syndromes with any logical combination of physical abnormalities. A descriptive title and full references are also provided on request. Similar systems would be applicable to other medical specialties.This publication has 5 references indexed in Scilit:
- The Greig polysyndactyly craniofacial dysmorphism syndrome: Variable expression in a familyEuropean Journal of Pediatrics, 1981
- Center for Birth Defects Information Services.1980
- Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: A new syndromeAmerican Journal of Medical Genetics, 1980
- A familial syndrome of cranial, facial, oral and limb anomaliesClinical Genetics, 1976