Detection of heterozygousSMN1 deletions in SMA families using a simple fluorescent multiplex PCR method | Journal of Medical Genetics
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Tissue differences in the exosomal/small extracellular vesicle proteome and their potential as indicators of altered tissue metabolism - ScienceDirect
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Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.
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
Heterozygosity deficiency in type I patients by marker C212 and C272.... | Download Scientific Diagram
Combined analysis of SMN, NAIP and microsatellite markers in... | Download Table
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
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
Two independent mutations of the SMN1 gene in the same spinal muscular atrophy family branch: Lessons for carrier diagnosis | Genetics in Medicine
C-212-400 Maritime Patrol Aircraft - Airforce Technology
Analysis of the acrolein-modified sites of apolipoprotein B-100 in LDL - ScienceDirect
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Prevalence of SMN1 deletion and duplication in carrier and normal populations: implication for genetic counselling | Journal of Medical Genetics
PDF) Missense Mutations in Exon 6 of the Survival Motor Neuron Gene in Patients with Spinal Muscular Atrophy (SMA)
Application of the Cre/lox System to Construct Auxotrophic Markers for Quantitative Genetic Analyses in Fusarium graminearum | SpringerLink
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IJMS | Free Full-Text | Analysis of Dormancy-Associated Transcriptional Networks Reveals a Shared Quiescence Signature in Lung and Colorectal Cancer
Heterozygosity deficiency in type I patients by marker C212 and C272.... | Download Scientific Diagram
Somatic mosaicism for a heterozygous deletion of the survival motor neuron (SMN1) gene | European Journal of Human Genetics
