A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)

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Publication year
1996
Author(s)
Hofstra, R.M.
Osinga, J.
Sindhunata, G.T.
Wu, Y.
Kamsteeg, E.J.
Stulp, R.P.
Ravenswaaij-Arts, C.M.A. van
Majoor-Krakauer, D.F.
Angrist, M.
Chakravarti, A.
Meijers, C.C.A.J.
Buijs, C.
Source
Nature Genetics, 12, (1996), pp. 445-447
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/150685   https://hdl.handle.net/2066/150685
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