1. Congenital Deafness: A New Approach to Early Detection Through a High Risk Register;Black,1971
2. Black, F. O., Sando, I., Wagner, J. A., and Hemenway, W. G.: A 13-15 (Dx) trisomy with middle and inner ear anomalies. To be published.
3. The genetics of childhood deafness;Brown,1967
4. Cytomegalovirus in the inner ear;Davis;Case report and electron microscopic study. Ann. Otol.,1969
5. Downs, M. P.: A critical approach to newborn hearing screening and the high risk register. Paper presented at Institute on “Earlier Detection and Treatment of Handicapping Conditions in Children,” Berkeley, California, May 6, 1970.