Exploring the genetic basis of 3MC syndrome: Findings in 12 further families.
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COLEC10 is mutated in 3MC patients and regulates early craniofacial development.Zebrafish models of orofacial clefts.Complement regulation and kidney diseases: recent knowledge of the double-edged roles of complement activation in nephrology.Analysis of Factor D Isoforms in Malpuech-Michels-Mingarelli-Carnevale Patients Highlights the Role of MASP-3 as a Maturase in the Alternative Pathway of Complement.Decreased expression of predicts poor overall survival in patients with hepatocellular carcinoma
P2860
Exploring the genetic basis of 3MC syndrome: Findings in 12 further families.
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2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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Exploring the genetic basis of 3MC syndrome: Findings in 12 further families.
@en
Exploring the genetic basis of 3MC syndrome: Findings in 12 further families.
@nl
type
label
Exploring the genetic basis of 3MC syndrome: Findings in 12 further families.
@en
Exploring the genetic basis of 3MC syndrome: Findings in 12 further families.
@nl
prefLabel
Exploring the genetic basis of 3MC syndrome: Findings in 12 further families.
@en
Exploring the genetic basis of 3MC syndrome: Findings in 12 further families.
@nl
P2093
P2860
P356
P1476
Exploring the genetic basis of 3MC syndrome: Findings in 12 further families
@en
P2093
Deepthi de Silva
Elena Chervinsky
Jill Clayton-Smith
Jill Urquhart
Mohnish Suri
Nicole Revencu
Rebecca Roberts
Romesh Gunasekera
Sanjeev Bhaskar
Sheela Nampoothiri
P2860
P304
P356
10.1002/AJMG.A.37564
P407
P577
2016-01-20T00:00:00Z