Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories.
about
Evolving health care through personal genomics.Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations.Ciliopathies: Genetics in Pediatric Medicine.Implementing non-invasive prenatal testing into publicly funded antenatal screening services for Down syndrome and other conditions in Aotearoa New Zealand.Views of the obstetric profession on non-invasive prenatal testing in Aotearoa New Zealand: A national survey.
P2860
Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories.
description
2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年学术文章
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2014年學術文章
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2014年學術文章
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2014年學術文章
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name
Implementation of whole genome ...... natal testing in laboratories.
@en
type
label
Implementation of whole genome ...... natal testing in laboratories.
@en
prefLabel
Implementation of whole genome ...... natal testing in laboratories.
@en
P2093
P2860
P1476
Implementation of whole genome ...... natal testing in laboratories.
@en
P2093
Brigitte H Faas
Djie Tjwan Thung
Jayne Hehir-Kwa
Lean Beulen
P2860
P304
P356
10.1586/14737159.2015.973857
P577
2014-10-27T00:00:00Z