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.), Making our way: Promoting self-competence among children and youth with disabilities. Baltimore: Brookes.

Turnbull, H. R., & Turnbull, A. P. (Eds.). (1985). Parents speak out: Then and now. Columbus, OH: Merrill.

United States Commission on Civil Rights. (1986). Protection of handicapped newborns: Hearing held in Washington, DC, June 26-21, 1986 (Vol. II). Washington, DC: U.S. Government Printing Office.

University of Pittsburgh Office of Child Development. (1991). Black families: An inquiry into the issues. Developments, 5(1), 5-8.

Upshur, С. C. (1982). Respite care for mentally retarded and other disabled populations: Program models and family needs. Mental Retardation, 20, 2-6.

Upshur, С. C. (1991). Families and the community service maze. In M. Seligman (Ed.), The family with a handicapped child [2nd ed., pp. 91-118). Boston: Allyn & Bacon.

Vadasy, P. F (1986). Single mothers: Asocial phenomenon and population in need. In R. R. Fewell & P. F Vadasy (Eds.), Families of handicapped children (pp. 221-249). Austin, Texas: Pro-Ed.

Vadasy, P. F, & Fewell, R. R. (1986). Mothers of deaf-blind children. In R. R. Fewell & R F Vadasy (Eds.), Families of handicapped children (pp. 121-148). Austin, TX: Pro-Ed.

Vadasy, P. Е, Fewell, R. R., & Meyer, D. J. (1986). Grandparents of children with special needs: Insights into their experiences and concerns. Journal of the Division for Early Childhood, 10, 36-44.

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. Topics in Early Childhood Education, 6, 16-31.

Vadasy, P. E, Fewell, R. R., Meyer, D. J., & Greenberg, M. T. (1985). Supporting fathers of handicapped young children: Preliminary findings of program effects. Analysis and Intervention in Developmental Disabilities, 5, 125-137.

Varekamp, M. A., Suurmeijer, R, Rosendaal, E R., Dijck, H., Uriends, A., & Briet, E. (1990). Family burden in families with a hemophilic child. Family Systems Medicine, 8, 291-301.

Vasta, R. (1982). Strategies and techniques of child study. New York: Academic Press.

Vincent, L. J., & Salisbury, G. L. (1988). Changing economic and social influences on family involvement. Topics in Early Childhood Special Education, 12, 48-59.

Visher, E., & Visher, J. (1988). Old loyalties new ties: Therapeutic strategies with step families. New York: Brunner/Mazel.

Von Bertalanffy, L. (1968). General systems theory. New York: Braziller.

Voysey, M. (1972). Impression management by parents with disabled children. Journal of Health and Social Behavior, 13, 80-89.

Voysey, M. (1975). A constant burden: The reconstitution of family life. London: Routledge & Kegan Paul.

Waechter, E. H. (1977). Bonding problems of infants with congenital anomalies. Nursing Forum, 16, 229-318.

Waisbren, E. (1980). Parents\' reactions after the birth of a developmentally disabled child. American Journal of Mental Deficiency, 84, 345-351.

Waitzkin, H. (1985). Information giving in medical care. Journal of Health and Social Behavior, 26, 81-101.

Waitzman, N. J., Romano, P. S., Scheffler, R. M., & Harris, J. A. (1995, September 22). Morbidity and mortality weekly report. Atlanta: Centers for Disease Control.

Walker, J. H. (1971). Spina bifida – and the parents. Developmental Medicine and Child Neurology, 13, 462-476.

Wallinga, C, Paquio, L., & Skeen, P. (1987). When a brother or sister is ill. Psychology Today, 42, 43.

Walsh, E (1989). The family in later life. In B. Garter & M. McGoldrick (Eds.), The changing family life cycle (2nd ed., pp. 311-332). Needham Heights, MA: Allyn & Bacon.

Wasow, M., & Wilder, L. (1983). Reflections on professionals\' attitudes toward the severely mentally retarded and the chronically mentally ill: Implications for parents. Family Therapy, 10, 299-308.

Перейти на страницу:

Похожие книги