Variations of CITED2 are associated with congenital heart disease (CHD) in Chinese population.
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PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger SyndromeFGFR2 mutation in 46,XY sex reversal with craniosynostosisA Molecular Study of Pediatric Spindle and Sclerosing Rhabdomyosarcoma: Identification of Novel and Recurrent VGLL2-related Fusions in Infantile Cases.Functional Analyses of a Novel CITED2 Nonsynonymous Mutation in Chinese Tibetan Patients with Congenital Heart Disease.Targeting CITED2 for Angiogenesis in Obesity and Insulin Resistance.
P2860
Variations of CITED2 are associated with congenital heart disease (CHD) in Chinese population.
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2014 nî lūn-bûn
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2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
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2014 թվականի մայիսին հրատարակված գիտական հոդված
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2014年の論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年论文
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name
Variations of CITED2 are assoc ...... e (CHD) in Chinese population.
@ast
Variations of CITED2 are assoc ...... e (CHD) in Chinese population.
@en
type
label
Variations of CITED2 are assoc ...... e (CHD) in Chinese population.
@ast
Variations of CITED2 are assoc ...... e (CHD) in Chinese population.
@en
prefLabel
Variations of CITED2 are assoc ...... e (CHD) in Chinese population.
@ast
Variations of CITED2 are assoc ...... e (CHD) in Chinese population.
@en
P2093
P2860
P1433
P1476
Variations of CITED2 are assoc ...... e (CHD) in Chinese population.
@en
P2093
Congmin Li
Fengyu Wang
Qiaolian Wen
Sainan Tan
Xiaomei Zhu
P2860
P304
P356
10.1371/JOURNAL.PONE.0098157
P407
P577
2014-05-21T00:00:00Z