Variants of uncertain significance in newborn screening disorders: implications for large-scale genomic sequencing.
about
Genomic newborn screening: public health policy considerations and recommendations.Array comparative genomic hybridization and genomic sequencing in the diagnostics of the causes of congenital anomalies.Reassessment of Genomic Sequence Variation to Harmonize Interpretation for Personalized Medicine.Exploring the importance of case-level clinical information for variant interpretation.
P2860
Variants of uncertain significance in newborn screening disorders: implications for large-scale genomic sequencing.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Variants of uncertain signific ...... arge-scale genomic sequencing.
@en
type
label
Variants of uncertain signific ...... arge-scale genomic sequencing.
@en
prefLabel
Variants of uncertain signific ...... arge-scale genomic sequencing.
@en
P2093
P2860
P356
P1433
P1476
Variants of uncertain signific ...... arge-scale genomic sequencing.
@en
P2093
Alekhya Narravula
Madhuri Hegde
S Hussain Askree
P2860
P2888
P356
10.1038/GIM.2016.67
P407
P577
2016-06-16T00:00:00Z
P6179
1033937844