Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses

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Title:	Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses
Author(s):	Wuyts, W.; Hul, W. van; Boulle, K. de; Hendrickx, J.J.; Bakker, E.; Vanhoenacker, F.; Mollica, F.; Ludecke, H.J.; Sayli, B.S.; Pazzaglia, U.E.; Mortier, G.R.; Hamel, B.C.J. ; Conrad, E.U.; Matsushita, M.; Raskind, W.H.; Willems, P.J.
Publication year:	1998
Source:	American Journal of Human Genetics, vol. 62, (1998), pp. 346-354
Number of Pages:	9 p.
ISSN:	0002-9297
DOI:	https://doi.org/10.1086/301726
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/166814
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Subject:	Clinical description and delineation of genetic syndromes Klinische beschrijving en moleculaire definiëring van genetische syndromen
Organization:	Otorhinolaryngology Human Genetics
Journal title:	American Journal of Human Genetics
Volume:	vol. 62
Page start:	p. 346
Page end:	p. 354