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Conference Paper: Recurrent de novo missense mutations in PP1CB cause a novel rasopathy closely resembling Noonan syndrome with loose anagen hair (Reviewer choice)

TitleRecurrent de novo missense mutations in PP1CB cause a novel rasopathy closely resembling Noonan syndrome with loose anagen hair (Reviewer choice)
Authors
Gripp, KWAldinger, KABennett, JBaker, LTusi, JPowell-Hamilton, NStabley, DSol-Church, KTimms, ADobyns, WBde Man, ALarson, ASpruijt, LKoolen, DStevens, SJCStegmann, APANillesen, MWNorrhock, HVBelien, MNellist, MVerheijen, FWilems, PJChung, BHYDubbs, HBhoj, ESantani, AMcDougall, CZackai, EHRinne, TKWessels, MW
Issue Date2016
Citation
The 2016 Joint Meeting of the Asian Society for Pediatric Research and Faculty of Medicine Ramathibodi Hospital (ASPR 2016), Bangkok, Thailand, 9-11 November 2016. How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/236474

 

DC FieldValueLanguage
dc.contributor.authorGripp, KW-
dc.contributor.authorAldinger, KA-
dc.contributor.authorBennett, J-
dc.contributor.authorBaker, L-
dc.contributor.authorTusi, J-
dc.contributor.authorPowell-Hamilton, N-
dc.contributor.authorStabley, D-
dc.contributor.authorSol-Church, K-
dc.contributor.authorTimms, A-
dc.contributor.authorDobyns, WB-
dc.contributor.authorde Man, A-
dc.contributor.authorLarson, A-
dc.contributor.authorSpruijt, L-
dc.contributor.authorKoolen, D-
dc.contributor.authorStevens, SJC-
dc.contributor.authorStegmann, APA-
dc.contributor.authorNillesen, MW-
dc.contributor.authorNorrhock, HV-
dc.contributor.authorBelien, M-
dc.contributor.authorNellist, M-
dc.contributor.authorVerheijen, F-
dc.contributor.authorWilems, PJ-
dc.contributor.authorChung, BHY-
dc.contributor.authorDubbs, H-
dc.contributor.authorBhoj, E-
dc.contributor.authorSantani, A-
dc.contributor.authorMcDougall, C-
dc.contributor.authorZackai, EH-
dc.contributor.authorRinne, TK-
dc.contributor.authorWessels, MW-
dc.date.accessioned2016-11-25T00:53:56Z-
dc.date.available2016-11-25T00:53:56Z-
dc.date.issued2016-
dc.identifier.citationThe 2016 Joint Meeting of the Asian Society for Pediatric Research and Faculty of Medicine Ramathibodi Hospital (ASPR 2016), Bangkok, Thailand, 9-11 November 2016.-
dc.identifier.urihttp://hdl.handle.net/10722/236474-
dc.languageeng-
dc.relation.ispartofAsian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016-
dc.titleRecurrent de novo missense mutations in PP1CB cause a novel rasopathy closely resembling Noonan syndrome with loose anagen hair (Reviewer choice)-
dc.typeConference_Paper-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.authorityChung, BHY=rp00473-
dc.identifier.hkuros270659-

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