The use of whole-exome sequencing to disentangle complex phenotypes
about
Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study.Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorderA novel mutation in nuclear prelamin a recognition factor-like causes diffuse pulmonary arteriovenous malformationsImplementation of genomic medicine in Sri Lanka: Initial experience and challenges.DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport.Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease.
P2860
The use of whole-exome sequencing to disentangle complex phenotypes
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
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
@zh
2015年學術文章
@zh-hant
name
The use of whole-exome sequencing to disentangle complex phenotypes
@ast
The use of whole-exome sequencing to disentangle complex phenotypes
@en
type
label
The use of whole-exome sequencing to disentangle complex phenotypes
@ast
The use of whole-exome sequencing to disentangle complex phenotypes
@en
prefLabel
The use of whole-exome sequencing to disentangle complex phenotypes
@ast
The use of whole-exome sequencing to disentangle complex phenotypes
@en
P2093
P2860
P356
P1476
The use of whole-exome sequencing to disentangle complex phenotypes
@en
P2093
Caroline Pao
Chiara Bacchelli
Elisabeth Rosser
Estelle Chanudet
Francesco Lescai
Horia C Stanescu
Hywel J Williams
John R Hurst
Louise Ocaka
P2860
P2888
P304
P356
10.1038/EJHG.2015.121
P50
P577
2015-06-10T00:00:00Z