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Detection of heterozygousSMN1 deletions in SMA families using a simple fluorescent multiplex PCR method | Journal of Medical Genetics
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Heterozygosity deficiency in type I patients by marker C212 and C272.... | Download Scientific Diagram
PDF) 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
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Heterozygosity deficiency in type I patients by marker C212 and C272.... | Download Scientific Diagram
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Prevalence of SMN1 deletion and duplication in carrier and normal populations: implication for genetic counselling | Journal of Medical Genetics
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Heterozygosity deficiency in type I patients by marker C212 and C272.... | Download Scientific Diagram
Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.
Linkage map of microsatellite markers used for BC 2 F 2 QTL analysis.... | Download Scientific Diagram
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a) Pedigree and haplotype analysis of the polymorphic multicopy marker... | Download Scientific Diagram
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Example of noninformative alleles in an SMA family. Markers C212 (upper... | Download Scientific Diagram
PDF) Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal Muscular Atrophy
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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 | Genetic Testing and Molecular Biomarkers
