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J.EJMG.2012.01.007
J.EJMG.2012.01.007
http://dx.doi.org/10.1016/J.EJMG.2012.01.007
De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: a genomics approach to personalized medicine.
P356
Q30525587-9B3FB01E-5B5D-414E-B97F-9E109FA7F42D
P356
J.EJMG.2012.01.007
http://dx.doi.org/10.1016/J.EJMG.2012.01.007