Newborn screening for citrin deficiency and carnitine uptake defect using second-tier molecular tests
about
Novel two-step derivation method for the synchronous analysis of inherited metabolic disorders using urine.Web-based newborn screening system for metabolic diseases: machine learning versus clinicians.Fatty Acid oxidation disorders in a chinese population in taiwan.Clinical chemistry and dried blood spots: increasing laboratory utilization by improved understanding of quantitative challenges.
P2860
Newborn screening for citrin deficiency and carnitine uptake defect using second-tier molecular tests
description
2013 nî lūn-bûn
@nan
2013 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի փետրվարին 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
Newborn screening for citrin d ...... ng second-tier molecular tests
@ast
Newborn screening for citrin d ...... ng second-tier molecular tests
@en
Newborn screening for citrin d ...... ng second-tier molecular tests
@nl
type
label
Newborn screening for citrin d ...... ng second-tier molecular tests
@ast
Newborn screening for citrin d ...... ng second-tier molecular tests
@en
Newborn screening for citrin d ...... ng second-tier molecular tests
@nl
prefLabel
Newborn screening for citrin d ...... ng second-tier molecular tests
@ast
Newborn screening for citrin d ...... ng second-tier molecular tests
@en
Newborn screening for citrin d ...... ng second-tier molecular tests
@nl
P2093
P2860
P50
P356
P1433
P1476
Newborn screening for citrin d ...... ng second-tier molecular tests
@en
P2093
Li-Yun Wang
Nien-I Chen
Pin-Wen Chen
Shu-Chuan Chiang
P2860
P2888
P356
10.1186/1471-2350-14-24
P577
2013-02-10T00:00:00Z
P5875
P6179
1043927049