Targeted screening and validation of copy number variations.
about
Appraisal of the technologies and review of the genomic landscape of ductal carcinoma in situ of the breastSystematic biases in DNA copy number originate from isolation proceduresMethods for applying accurate digital PCR analysis on low copy DNA samples.Current analysis platforms and methods for detecting copy number variationQuantitative multiplex PCR of short fluorescent fragments for the detection of large intragenic POLG rearrangements in a large French cohort.Quantitative PCR: an alternative approach to detect common copy number alterations in multiple myeloma.Accurate clinical detection of exon copy number variants in a targeted NGS panel using DECoN.The Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Epilepsy in Paediatric Patients.Frequency of KLK3 gene deletions in the general population.Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond-Blackfan anemia.An MLPA-based strategy for discrete CNV genotyping: CNV-miRNAs as an example.
P2860
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P2860
Targeted screening and validation of copy number variations.
description
article científic
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article scientifique
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articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Targeted screening and validation of copy number variations.
@en
Targeted screening and validation of copy number variations.
@nl
type
label
Targeted screening and validation of copy number variations.
@en
Targeted screening and validation of copy number variations.
@nl
prefLabel
Targeted screening and validation of copy number variations.
@en
Targeted screening and validation of copy number variations.
@nl
P1476
Targeted screening and validation of copy number variations
@en
P2093
Karlijn van der Ven
Shana Ceulemans
P304
P356
10.1007/978-1-61779-507-7_15
P407
P577
2012-01-01T00:00:00Z