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  1. Article

    Open Access

    Fine map** of the 9q31 Hirschsprung’s disease locus

    Hirschsprung’s disease (HSCR) is a congenital disorder characterised by the absence of ganglia along variable lengths of the intestine. The RET gene is the major HSCR gene. Reduced penetrance of RET mutations and...

    C. S. Tang, Y. Sribudiani, X. P. Miao, A. R. de Vries, G. Burzynski… in Human Genetics (2010)

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