Sarfarazi M, Quarrell O W, Wolak G, Harper P S
Institute of Medical Genetics, University of Wales College of Medicine, Cardiff, United Kingdom.
Am J Med Genet. 1987 Dec;28(4):999-1006. doi: 10.1002/ajmg.1320280427.
A microcomputer program has been designed to maintain a large data base for Huntington disease. This program facilitates such data manipulation as adding, altering, retrieving, deleting, and printing pedigrees. The program is self-contained and has a risk-calculating routine built in which automatically provides both the Mendelian and age-modified risks. This package is capable of printing the pedigrees on a simple printer or, alternatively, creates an output-file which can be used with a dedicated plotting program for drawing the pedigrees and their data on a plotter. The program has a routine which can provide a series of statistical data from the register including age-of-onset, diagnosis, death, and other useful information.