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A c.1019A > G mutation inFGFR2, which predicts p.Tyr340Cys, in a lethally malformed fetus with Pfeiffer syndrome and multiple pterygia

Baynam, G., Smith, N. and Goldblatt, J. (2008) A c.1019A > G mutation inFGFR2, which predicts p.Tyr340Cys, in a lethally malformed fetus with Pfeiffer syndrome and multiple pterygia. American Journal of Medical Genetics Part A, 146A (17). pp. 2301-2303.

Link to Published Version: http://dx.doi.org/10.1002/ajmg.a.32443
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Abstract

Research Letter

Publication Type: Journal Article
Publisher: Wiley-Liss Inc
Copyright: © 2008 Wiley-Liss, Inc.
URI: http://researchrepository.murdoch.edu.au/id/eprint/25235
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