Exome sequencing identifies a de novo mutation of CTNNB1 gene in a patient mainly presented with retinal detachment, lens and vitreous opacities, microcephaly, and developmental delay: Case report and literature review.
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Exome sequencing identifies a de novo mutation of CTNNB1 gene in a patient mainly presented with retinal detachment, lens and vitreous opacities, microcephaly, and developmental delay: Case report and literature review.
description
2017 nî lūn-bûn
@nan
2017 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2017 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
name
Exome sequencing identifies a ...... report and literature review.
@ast
Exome sequencing identifies a ...... report and literature review.
@en
type
label
Exome sequencing identifies a ...... report and literature review.
@ast
Exome sequencing identifies a ...... report and literature review.
@en
prefLabel
Exome sequencing identifies a ...... report and literature review.
@ast
Exome sequencing identifies a ...... report and literature review.
@en
P2093
P2860
P31
P921
P1433
P1476
Exome sequencing identifies a ...... report and literature review.
@en
P2093
Guoqiang Li
Tingting Yu
Xiumin Wang
P2860
P356
10.1097/MD.0000000000006914
P407
P5008
P577
2017-05-01T00:00:00Z