Consultas e Referências

ALMEIDA-FILHO, N, Mari LL et al. Brazilian Mulicentric Study of Psychiatric Morbidity Br J Psychiatry. 1997.

AL SEMAAN Y. Schizoaffective disorder in a fragile-X carrier. Aust N Z J Psychiatry, 1999.

BUTLER Mg et al. An trhopometric comparison of mentally retarded males with and without the fragile X syndrome. Am J Med Genet, 1991.

_____________, GUPTA R & SINGH DN. A 15 item checklist for screening mentally retarded males for the fragile X syndrome. Clin Genet, 1991.

CURFS LMG et al. Intelligence and cognitive in tha fragile X syndrome: a longitudinal study in 18 fra (X)boys. J Med Genet, 1989.

EICHLER EE, RICHARDS S, RA & Nelson DL. Fine Structure of the human FMR1 gene. Hum Mol Genet, 1993.

GRADOW KD, POLING AG. Pharmacotherapy and Mental Retardation. College Hill Press, Boston, 1998.

HAGERMAN, R. J. Fragile X Syndrome - Molecular and Clinical Insights and Treatment Issues. In: West J. Med, p. 129-137. Feb/1997.

_____________. Diretrices de Asistencia en el Síndrome X Frágil. In: El Sindrome X Frágil - Material Educativo de la Fundación Nacional de X Frágil de Estados Unidos, p.83-98. Publ. IMSERSO. Madri, 1998.

KRAMER PD. Listening to Prozac. Viking Press, New York, 1993.

LACHIEWICZ AM, Gullion CM, SPIRIDIGLIOZZI GA & Aylsworth AS. Declining IQs of young males with x syndrome. Am J Méd Retarde. 1987.

LOEHR JP, SYNHORST DP, WOLFE RR & HAGERMAN RJ. Aortic root dialtation and mitral valve prolapse in the fragile X syndrome. Am J Méd Fenet, 1991.

LUBS HÁ. A marker-x cromosome. Am J Hum Fenet, 1969.

MCKUSICK VA, FRANCOMO CA & ANTONARAKIS SE. Mendelian Inheritance in Man. Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes. 1990, Baltimore, The Johns Hopkins University Press.

MORGANTE, A . V. A Síndrome do Cromossomo X-Frágil. In: Estudos Avançados-Coleção Documentos Série Especial- Ciclo de Conferências Temáticas - 1.3. Publ. USP On line. Janeiro/1997.

NUSSBAUM RL & LEDBETTER DH. The fragile X syndrome. (1989) In : Scriver CR, Beaudet Al, Sly WS & Valle D. The Metabolic basics of Inherited Disease. 6 edicion. New York. NY. MC-Graw-Hill.

OTERO, Y. D. et alli. Síndrome de X Frágil y Discapacidad Mental Hereditária. Ministério de Sanidad Y Consumo. Madrid, 1999.

SHARFENAKER, S. et alli. An Integrated Approach to Intervention. In: Fragile X Syndrome: Diagnosis, Treatment and Research. Ed. Randi Jenssen Hagerman and Amy Cronister. Johns Hopkins University Press. Baltimore, 1996.

_________________. Características del Habla y del Lenguagje en el Síndrome X Frágil. In: El Sindrome X Frágil - Material Educativo de la Fundación Nacional de X Frágil de Estados Unidos, p99 - 113. Publ. IMSERSO. Madri, 1998.

MELIS MA; ADDIS M; Lepiani C; CONGEDDU E; COSSU P; CAO A. A strategy for fragile-X carrier screening. Genet Test, 1999.

SINGH R; SUTHERLAND GR; MANSON J. Partial seizures with focal epileptogenic electroencephalographic patterns in three related female patients with fragile-X syndrome. J Child Neurol, 1999.

TRANEBJAERG L. Genetic causes of mental retardation--diagnostic possibilities. Tidsskr Nor Laegeforen, 1999.

Turk J (1992) Fragile X syndrome and folic acid. In Hagerman RJ & McKenzie P (Eds) 1992 International Fragile X Conference Proceedings. The National Fragile X Foundation & Spectra Publishing, Dillon, CO. pp 195-200.

YORK A; von Fraunhofer N; TURK J; SEDGWICK P. Fragile-X syndrome, Down's syndrome and autism: awareness and knowledge amongst special educators. J Intellect Disabil Res, 1999.

WERRY JS, AMAN MG. Practitioner's Guide to Psychoactive Drugs for Children & Adolescents. Plenum Medical Book Company, New York,1993.