Gender Ratios in Children with Reading Disability and Their Affected Relatives

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References

Carter, C.O. (1969). Genetics of common disorders. British Medical Bulletin, 25, 52–57.

Carter, C.O. (1973). Multifactorial genetic disease. In V.A. McKusick & R. Clairbome (Eds.), Medical genetics (pp. 199–208). New York: HP Publishing.

DeFries, J.C. , & Decker, S.N. (1982). Genetic aspects of reading disability: A family study. In R.N. Malatesha & P.G. Aaron (Eds.), Reading disorders: Varieties and treatments (pp. 255–279). New York: Academic Press.

Finucci, J.M. , & Childs, B. (1981). Are there really more dyslexic boys than girls? In A. Ansara , N. Geschwind , A. Galaburda , M. Albert , & N. Gartrell. (Eds.), Sex differences in dyslexia (pp. 1–9). Towson, MD: Orton Dyslexia Society.

Finucci, J.M. , Gottfredson, L.S. , & Childs, B. (1985). A follow-up study of dyslexic boys. Annals of Dyslexia, 35, 117–136.

Hallgren, B. (1950). Specific dyslexia: A clinical and genetic study. Acta Psychiatrica et Neurologica Scandinavica, 65 (Supplement), 1–287.

Vogler, G.P. , DeFries, J.C. , & Decker, S.N. (1985). Family history as an indicator of risk for reading disability. Journal of Learning Disabilities, 18, 419–421.