Analysis of the acrolein-modified sites of apolipoprotein B-100 in LDL - ScienceDirect
Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.
Heterozygosity deficiency in type I patients by marker C212 and C272.... | Download Scientific Diagram
Curcumin derivative C212 inhibits Hsp90 and eliminates both growing and quiescent leukemia cells in deep dormancy | Cell Communication and Signaling | Full Text
a) Pedigree and haplotype analysis of the polymorphic multicopy marker... | Download Scientific Diagram
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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
Prevalence of SMN1 deletion and duplication in carrier and normal populations: implication for genetic counselling | Journal of Medical Genetics
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Detection of heterozygousSMN1 deletions in SMA families using a simple fluorescent multiplex PCR method | Journal of Medical Genetics
Somatic mosaicism for a heterozygous deletion of the survival motor neuron (SMN1) gene | European Journal of Human Genetics
Linkage map of microsatellite markers used for BC 2 F 2 QTL analysis.... | Download Scientific Diagram
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Tissue differences in the exosomal/small extracellular vesicle proteome and their potential as indicators of altered tissue metabolism - ScienceDirect
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