An overview of mutation detection methods in genetic disorders.
about
Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathiesPostnatal and non-invasive prenatal detection of β-thalassemia mutations based on Taqman genotyping assays.Isocitrate dehydrogenase mutations in myeloid malignancies.Development and validation of a whole-exome sequencing test for simultaneous detection of point mutations, indels and copy-number alterations for precision cancer care.Human Immunodeficiency Virus Resistance Testing Technologies and Their Applicability in Resource-Limited Settings of Africa.Surface Enhanced Raman Spectroscopy (SERS) for the Multiplex Detection of Braf, Kras, and Pik3ca Mutations in Plasma of Colorectal Cancer Patients.
P2860
An overview of mutation detection methods in genetic disorders.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on August 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
An overview of mutation detection methods in genetic disorders.
@en
An overview of mutation detection methods in genetic disorders.
@nl
type
label
An overview of mutation detection methods in genetic disorders.
@en
An overview of mutation detection methods in genetic disorders.
@nl
prefLabel
An overview of mutation detection methods in genetic disorders.
@en
An overview of mutation detection methods in genetic disorders.
@nl
P2860
P1476
An overview of mutation detection methods in genetic disorders.
@en
P2093
Nejat Mahdieh
P2860
P304
P577
2013-08-01T00:00:00Z