Pedigree of the SMA family used to validate the multiplex PCR. Filled... | Download Scientific Diagram
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
Identification and development of a core set of informative genic SNP markers for assaying genetic diversity in Chinese cabbage | SpringerLink
Application of the Cre/lox System to Construct Auxotrophic Markers for Quantitative Genetic Analyses in Fusarium graminearum | SpringerLink
Prevalence of SMN1 deletion and duplication in carrier and normal populations: implication for genetic counselling | Journal of Medical Genetics
Analysis of the acrolein-modified sites of apolipoprotein B-100 in LDL - ScienceDirect
Curcumin derivative C212 inhibits Hsp90 and eliminates both growing and quiescent leukemia cells in deep dormancy | Cell Communication and Signaling | Full Text
Heterozygosity deficiency in type I patients by marker C212 and C272.... | Download Scientific Diagram
Linkage map of microsatellite markers used for BC 2 F 2 QTL analysis.... | Download Scientific Diagram
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
Curcumin derivative C212 inhibits Hsp90 and eliminates both growing and quiescent leukemia cells in deep dormancy | Cell Communication and Signaling | Full Text
Two independent mutations of the SMN1 gene in the same spinal muscular atrophy family branch: Lessons for carrier diagnosis | Genetics in Medicine
miR-322/-503 rescues myoblast defects in myotonic dystrophy type 1 cell model by targeting CUG repeats | Cell Death & Disease
De novo rearrangements found in 2% of index patients with spinal muscular atrophy: mutational mechanisms, parental origin, mutation rate, and implications for genetic counseling. - Abstract - Europe PMC
Somatic mosaicism for a heterozygous deletion of the survival motor neuron (SMN1) gene | European Journal of Human Genetics