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Prenatal Diagnosis
|
October 19, 2005
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination
Antonio Percesepe, Maurizio Ferrari, Domenico Coviello, et al.
Genes
|
June 27, 2024
An Unclassified Deletion Involving the Proximal Short Arm of Chromosome 10: A New Syndrome?
Graziano Santoro, Mariarosaria Incoronato, Edoardo Spagnoli, et al.
Clinical Chemistry and Laboratory Medicine
|
December 22, 2009
Integrated PCR amplification and detection processes on a Lab-on-Chip platform: a new advanced solution for molecular diagnostics
Barbara Foglieni, Angela Brisci, Floriana San Biagio, et al.
Clinical Chemistry and Laboratory Medicine
|
June 29, 2010
High resolution melting for the identification of mutations in the iron responsive element of the ferritin light chain gene
Emanuela Castiglioni, Nadia Soriani, Domenico Girelli, et al.
Cells
|
July 27, 2019
Microarray Approach Combined with ddPCR: An Useful Pipeline for the Detection and Quantification of Circulating Tumour dna Mutations
Silvia Galbiati, Francesco Damin, Lucia Ferraro, et al.
Electrophoresis
|
January 9, 2009
Dual-color microchip electrophoresis with single-photon avalanche diodes: application to mutation detection
Stefania Stenirri, Marina Cretich, Ivan Rech, et al.
Optics Express
|
November 18, 2014
Light-opals interaction modeling by direct numerical solution of Maxwell's equations
Alessandro Vaccari, Antonino Calà Lesina, Luca Cristoforetti, et al.
Micromachines
|
March 14, 2020
Photonic Crystal Stimuli-Responsive Chromatic Sensors: A Short Review
Andrea Chiappini, Lam Thi Ngoc Tran, Pablo Marco Trejo-García, et al.
Molecules (Basel, Switzerland)
|
March 6, 2021
Luminescent Ink Based on Upconversion of NaYF<sub>4</sub>:Er,Yb@MA Nanoparticles: Environmental Friendly Synthesis and Structural and Spectroscopic Assessment
T M Dung Cao, T T Giang Le, Sylvia Turrell, et al.
Human Molecular Genetics
|
July 30, 2015
High-throughput genetic characterization of a cohort of Brugada syndrome patients
Chiara Di Resta, Alessandro Pietrelli, Simone Sala, et al.
Page
of 19
Search research articles
Search
Showing results (71-80 of 186) with videos related to
Sort By:
Page
of 19
Prenatal Diagnosis
|
October 19, 2005
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination
Antonio Percesepe, Maurizio Ferrari, Domenico Coviello, et al.
Genes
|
June 27, 2024
An Unclassified Deletion Involving the Proximal Short Arm of Chromosome 10: A New Syndrome?
Graziano Santoro, Mariarosaria Incoronato, Edoardo Spagnoli, et al.
Clinical Chemistry and Laboratory Medicine
|
December 22, 2009
Integrated PCR amplification and detection processes on a Lab-on-Chip platform: a new advanced solution for molecular diagnostics
Barbara Foglieni, Angela Brisci, Floriana San Biagio, et al.
Clinical Chemistry and Laboratory Medicine
|
June 29, 2010
High resolution melting for the identification of mutations in the iron responsive element of the ferritin light chain gene
Emanuela Castiglioni, Nadia Soriani, Domenico Girelli, et al.
Cells
|
July 27, 2019
Microarray Approach Combined with ddPCR: An Useful Pipeline for the Detection and Quantification of Circulating Tumour dna Mutations
Silvia Galbiati, Francesco Damin, Lucia Ferraro, et al.
Electrophoresis
|
January 9, 2009
Dual-color microchip electrophoresis with single-photon avalanche diodes: application to mutation detection
Stefania Stenirri, Marina Cretich, Ivan Rech, et al.
Optics Express
|
November 18, 2014
Light-opals interaction modeling by direct numerical solution of Maxwell's equations
Alessandro Vaccari, Antonino Calà Lesina, Luca Cristoforetti, et al.
Micromachines
|
March 14, 2020
Photonic Crystal Stimuli-Responsive Chromatic Sensors: A Short Review
Andrea Chiappini, Lam Thi Ngoc Tran, Pablo Marco Trejo-García, et al.
Molecules (Basel, Switzerland)
|
March 6, 2021
Luminescent Ink Based on Upconversion of NaYF<sub>4</sub>:Er,Yb@MA Nanoparticles: Environmental Friendly Synthesis and Structural and Spectroscopic Assessment
T M Dung Cao, T T Giang Le, Sylvia Turrell, et al.
Human Molecular Genetics
|
July 30, 2015
High-throughput genetic characterization of a cohort of Brugada syndrome patients
Chiara Di Resta, Alessandro Pietrelli, Simone Sala, et al.
Page
of 19