A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations.
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A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations.
description
2017 nî lūn-bûn
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2017年の論文
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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年学术文章
@zh-cn
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2017年學術文章
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name
A quantitative cSMART assay fo ...... by GJB2 and SLC26A4 mutations.
@en
A quantitative cSMART assay fo ...... by GJB2 and SLC26A4 mutations.
@nl
type
label
A quantitative cSMART assay fo ...... by GJB2 and SLC26A4 mutations.
@en
A quantitative cSMART assay fo ...... by GJB2 and SLC26A4 mutations.
@nl
prefLabel
A quantitative cSMART assay fo ...... by GJB2 and SLC26A4 mutations.
@en
A quantitative cSMART assay fo ...... by GJB2 and SLC26A4 mutations.
@nl
P2093
P2860
P356
P1433
P1476
A quantitative cSMART assay fo ...... by GJB2 and SLC26A4 mutations.
@en
P2093
David S Cram
Dongyang Kang
Longxia Wang
Mengnan Xu
Mingyu Han
Shasha Huang
Wenlu Wang
Yanping Lu
P2860
P2888
P304
P356
10.1038/GIM.2017.54
P407
P577
2017-05-25T00:00:00Z