Development of new substrates for high-sensitive genotyping of minority mutated alleles

scientific article

Development of new substrates for high-sensitive genotyping of minority mutated alleles is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1002/ELPS.200800242
P8608Fatcat IDrelease_vm3vwftoobbd5kup4lmhr6ugsq
P698PubMed publication ID19053069

P2093author name stringLaura Cremonesi
Maurizio Ferrari
Silvia Galbiati
Francesco Damin
Gabriele Di Carlo
Marcella Chiari
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Enhanced sensitivity detection of protein immobilization by fluorescent interference on oxidized siliconQ44659356
Microarray-based method for genotyping of functional single nucleotide polymorphisms using dual-color fluorescence hybridizationQ44828874
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High-throughput mutational screening for beta-thalassemia by single-nucleotide extensionQ57079121
Different Approaches for Noninvasive Prenatal Diagnosis of Genetic Diseases Based on PNA-Mediated Enriched PCRQ58008255
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Optimisation of a silicon/silicon dioxide substrate for a fluorescence DNA microarrayQ80951561
P433issue23
P921main subjectgenotypingQ912147
P304page(s)4714-4722
P577publication date2008-12-01
P1433published inElectrophoresisQ3050608
P1476titleDevelopment of new substrates for high-sensitive genotyping of minority mutated alleles
P478volume29

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cites work (P2860)
Q34639858A new microarray substrate for ultra-sensitive genotyping of KRAS and BRAF gene variants in colorectal cancer
Q52883296COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma.
Q38002921Fetal DNA in maternal plasma: a noninvasive tool for prenatal diagnosis of beta-thalassemia.
Q58008242High-sensitive microarray substrates specifically designed to improve sensitivity for the identification of fetal paternally inherited sequences in maternal plasma

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