Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping platform
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Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technologyNew multiplex real-time PCR approach to detect gene mutations for spinal muscular atrophy.Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approachTargeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern Brazil.
P2860
Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping platform
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2013 nî lūn-bûn
@nan
2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Optimization of simultaneous s ...... OpenArray™ Genotyping platform
@ast
Optimization of simultaneous s ...... OpenArray™ Genotyping platform
@en
type
label
Optimization of simultaneous s ...... OpenArray™ Genotyping platform
@ast
Optimization of simultaneous s ...... OpenArray™ Genotyping platform
@en
prefLabel
Optimization of simultaneous s ...... OpenArray™ Genotyping platform
@ast
Optimization of simultaneous s ...... OpenArray™ Genotyping platform
@en
P2093
P2860
P356
P1433
P1476
Optimization of simultaneous s ...... OpenArray™ Genotyping platform
@en
P2093
Arthur Menino Castilho
Edi Lúcia Sartorato
Fábio Tadeu Arrojo Martins
Maria Carolina Costa Melo Svidnicki
Priscila Zonzini Ramos
P2860
P2888
P356
10.1186/1471-2350-14-112
P577
2013-10-24T00:00:00Z
P5875
P6179
1032533072