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Browsing by Author Chakravarti, A.
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Issue Date
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1996
A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)
Hofstra, R.M.
;
Osinga, J.
;
Sindhunata, G.T.
;
Wu, Y.
;
Kamsteeg, E.J.
, et al
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