Rebeca Martinez Hernandez
0000-0003-2479-1882
25 papers found
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Accuracy of Marker Analysis, Quantitative Real-Time Polymerase Chain Reaction, and Multiple Ligation-Dependent Probe Amplification to Determine SMN2 Copy Number in Patients with Spinal Muscular Atrophy
Ultrasound evaluation of fetal movements in pregnancies at risk for severe spinal muscular atrophy
The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor
The Developmental Pattern of Myotubes in Spinal Muscular Atrophy Indicates Prenatal Delay of Muscle Maturation:
Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene
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