Turnbull, A. R, & Turnbull, H. R., Ill (in press). An analysis of self-determination within a culturally responsive family systems perspective: Balancing the family mobile. In J. Sowers (Ed.),
Turnbull, H. R., & Turnbull, A. P. (Eds.). (1985).
United States Commission on Civil Rights. (1986).
University of Pittsburgh Office of Child Development. (1991). Black families: An inquiry into the issues.
Upshur, С. C. (1982). Respite care for mentally retarded and other disabled populations: Program models and family needs.
Upshur, С. C. (1991). Families and the community service maze. In M. Seligman (Ed.),
Vadasy, P. F (1986). Single mothers: Asocial phenomenon and population in need. In R. R. Fewell & P. F Vadasy (Eds.),
Vadasy, P. F, & Fewell, R. R. (1986). Mothers of deaf-blind children. In R. R. Fewell & R F Vadasy (Eds.),
Vadasy, P. Е, Fewell, R. R., & Meyer, D. J. (1986). Grandparents of children with special needs: Insights into their experiences and concerns.
Vadasy, R E, Fewell, R. R., Greenberg, M. Т., Desmond, N. L., & Meyer, D. J. (1986). Follow-up evaluation of the effects of involvement in the fathers program.
Vadasy, P. E, Fewell, R. R., Meyer, D. J., & Greenberg, M. T. (1985). Supporting fathers of handicapped young children: Preliminary findings of program effects.
Varekamp, M. A., Suurmeijer, R, Rosendaal, E R., Dijck, H., Uriends, A., & Briet, E. (1990). Family burden in families with a hemophilic child.
Vasta, R. (1982).
Vincent, L. J., & Salisbury, G. L. (1988). Changing economic and social influences on family involvement.
Visher, E., & Visher, J. (1988).
Von Bertalanffy, L. (1968).
Voysey, M. (1972). Impression management by parents with disabled children.
Voysey, M. (1975). A
Waechter, E. H. (1977). Bonding problems of infants with congenital anomalies.
Waisbren, E. (1980). Parents\' reactions after the birth of a developmentally disabled child.
Waitzkin, H. (1985). Information giving in medical
Waitzman, N. J., Romano, P. S., Scheffler, R. M., & Harris, J. A. (1995, September 22).
Walker, J. H. (1971). Spina bifida – and the parents.
Wallinga, C, Paquio, L., & Skeen, P. (1987). When a brother or sister is ill.
Walsh, E (1989). The family in later life. In B. Garter & M. McGoldrick (Eds.),
Wasow, M., & Wilder, L. (1983). Reflections on professionals\' attitudes toward the severely mentally retarded and the chronically mentally ill: Implications for parents.