scholarly article | Q13442814 |
P356 | DOI | 10.1002/ELPS.200800242 |
P8608 | Fatcat ID | release_vm3vwftoobbd5kup4lmhr6ugsq |
P698 | PubMed publication ID | 19053069 |
P2093 | author name string | Laura Cremonesi | |
Maurizio Ferrari | |||
Silvia Galbiati | |||
Francesco Damin | |||
Gabriele Di Carlo | |||
Marcella Chiari | |||
P2860 | cites work | Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS) | Q24635921 |
Characterization of a polymeric adsorbed coating for DNA microarray glass slides | Q33198684 | ||
A genotyping system capable of simultaneously analyzing >1000 single nucleotide polymorphisms in a haploid genome | Q33780777 | ||
A novel, sensitive detection system for high-density microarrays using dendrimer technology | Q33919922 | ||
DNA conformation on surfaces measured by fluorescence self-interference | Q34479864 | ||
Development of a universal probe for electronic microarray and its application in characterization of the Staphylococcus aureus polC gene | Q35870433 | ||
Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies | Q36247154 | ||
Prenatal diagnosis: progress through plasma nucleic acids | Q36673937 | ||
An overview of current microarray-based human globin gene mutation detection methods | Q36892393 | ||
MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis. | Q36986986 | ||
Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolism. | Q38317054 | ||
Beta thalassaemia mutations in Mediterranean populations. | Q38613699 | ||
An improved electronic microarray-based diagnostic assay for identification of MEFV mutations | Q40533811 | ||
Peptide nucleic acid (PNA). A DNA mimic with a peptide backbone | Q40760039 | ||
High-sensitivity detection of DNA hybridization on microarrays using resonance light scattering | Q43976941 | ||
Enhanced sensitivity detection of protein immobilization by fluorescent interference on oxidized silicon | Q44659356 | ||
Microarray-based method for genotyping of functional single nucleotide polymorphisms using dual-color fluorescence hybridization | Q44828874 | ||
Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma | Q47391690 | ||
Feasibility study for a microchip-based approach for noninvasive prenatal diagnosis of genetic diseases. | Q51596224 | ||
Beta-thalassemia microelectronic chip: a fast and accurate method for mutation detection. | Q51598367 | ||
Integrated strategy for fast and automated molecular characterization of genes involved in craniosynostosis. | Q51978338 | ||
Quantum dot bioconjugates for ultrasensitive nonisotopic detection. | Q54135557 | ||
Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of beta-thalassemia. | Q54543179 | ||
Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
High-throughput mutational screening for beta-thalassemia by single-nucleotide extension | Q57079121 | ||
Different Approaches for Noninvasive Prenatal Diagnosis of Genetic Diseases Based on PNA-Mediated Enriched PCR | Q58008255 | ||
Electric-field assisted immobilization and hybridization of DNA oligomers on thin-film microchips | Q58853392 | ||
The beta- and delta-thalassemia repository (Ninth Edition; Part I) | Q74519577 | ||
Zeptosens' protein microarrays: a novel high performance microarray platform for low abundance protein analysis | Q74581615 | ||
Optimisation of a silicon/silicon dioxide substrate for a fluorescence DNA microarray | Q80951561 | ||
P433 | issue | 23 | |
P921 | main subject | genotyping | Q912147 |
P304 | page(s) | 4714-4722 | |
P577 | publication date | 2008-12-01 | |
P1433 | published in | Electrophoresis | Q3050608 |
P1476 | title | Development of new substrates for high-sensitive genotyping of minority mutated alleles | |
P478 | volume | 29 |
Q34639858 | A new microarray substrate for ultra-sensitive genotyping of KRAS and BRAF gene variants in colorectal cancer |
Q52883296 | COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma. |
Q38002921 | Fetal DNA in maternal plasma: a noninvasive tool for prenatal diagnosis of beta-thalassemia. |
Q58008242 | High-sensitive microarray substrates specifically designed to improve sensitivity for the identification of fetal paternally inherited sequences in maternal plasma |
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