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  • Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome.

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Research Article
Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome.

Authors

    Citation

    Santos H, Mateus J, Leal MJ
    Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome.
    Journal of Medical Genetics 1988;25:204-205.

    Publication history

    • First published March 1, 1988.
    Online issue publication 
    January 18, 2017

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