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J.AJHG.2012.11.016
J.AJHG.2012.11.016
http://dx.doi.org/10.1016/J.AJHG.2012.11.016
Mutations in MEOX1, encoding mesenchyme homeobox 1, cause Klippel-Feil anomaly.
P356
Q36524761-93A347AC-6DFD-4375-AE22-8C2B91F61905
P356
J.AJHG.2012.11.016
http://dx.doi.org/10.1016/J.AJHG.2012.11.016