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JMG.27.7.426
JMG.27.7.426
http://dx.doi.org/10.1136/JMG.27.7.426
Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.
P356
Q33597984-8371C49F-1895-4A0B-A86F-072E67825A1C
P356
JMG.27.7.426
http://dx.doi.org/10.1136/JMG.27.7.426