Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders.
about
TUBB1 variants and human platelet traits.High-throughput sequencing for rapid diagnosis of inherited platelet disorders: a case for a European consensus.A comprehensive targeted next-generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopeniaPhenotype description and response to thrombopoietin receptor agonist in -related disorderTBXA2R gene variants associated with bleeding
P2860
Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
@wuu
2017年学术文章
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2017年学术文章
@zh-cn
2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年學術文章
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name
Introducing high-throughput se ...... inherited platelet disorders.
@en
Introducing high-throughput se ...... inherited platelet disorders.
@nl
type
label
Introducing high-throughput se ...... inherited platelet disorders.
@en
Introducing high-throughput se ...... inherited platelet disorders.
@nl
prefLabel
Introducing high-throughput se ...... inherited platelet disorders.
@en
Introducing high-throughput se ...... inherited platelet disorders.
@nl
P2093
P2860
P50
P1433
P1476
Introducing high-throughput se ...... n inherited platelet disorders
@en
P2093
Agustín Rodriguez-Alén
Anna E Marneth
Bert A van der Reijden
Carlos Aguilar
Hermenegildo González-García
Jesús M Hernández-Rivas
José R González-Porras
José Rivera
Kamila Janusz
Mónica Del Rey
P2860
P304
P356
10.3324/HAEMATOL.2017.171132
P50
P577
2017-10-05T00:00:00Z