about
An extended set of yeast-based functional assays accurately identifies human disease mutations.NGS Technologies as a Turning Point in Rare Disease Research , Diagnosis and Treatment.Whole-Genome Sequencing in Newborn Screening-Attitudes and Opinions of Bulgarian Pediatricians and Geneticists.A next-generation newborn screening pilot study: NGS on dried blood spots detects causal mutations in patients with inherited metabolic diseases.
P2860
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
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2015年學術文章
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name
Newborn screening and the era of medical genomics.
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Newborn screening and the era of medical genomics.
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type
label
Newborn screening and the era of medical genomics.
@ast
Newborn screening and the era of medical genomics.
@en
prefLabel
Newborn screening and the era of medical genomics.
@ast
Newborn screening and the era of medical genomics.
@en
P2860
P1476
Newborn screening and the era of medical genomics.
@en
P2093
Ludmila Francescatto
Nicholas Katsanis
P2860
P304
P356
10.1053/J.SEMPERI.2015.09.010
P577
2015-10-20T00:00:00Z