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De novo mutations in PLXND1 and REV3L cause Möbius syndrome.

dc.contributor.authorSORIA, L
dc.contributor.authorvan, Beusekom
dc.contributor.authorROSCIOLI, T
dc.contributor.authorIQBAL, Z
dc.contributor.authorGILISSEN, C
dc.contributor.authorHOISCHEN, A
dc.contributor.authorde, Brouwer
dc.contributor.authorERASMUS, C
dc.contributor.authorSCHUBERT, D
dc.contributor.authorBRUNNER, H
dc.contributor.authorPérez, Aytés
dc.contributor.authorMARIN, F
dc.contributor.authorTOMAS-ROCA, L
dc.contributor.authorAROCA, P
dc.contributor.authorKAYSERILI, H
dc.contributor.authorCARTA, A
dc.contributor.authorde, Wind
dc.contributor.authorPADBERG, GW
dc.contributor.authorvan, Bokhoven
dc.contributor.authorAltunoglu, UMUT
dc.contributor.authorTSAALBI-SHTYLIK, A
dc.contributor.authorJANSEN, JG
dc.contributor.authorSINGH, MK
dc.contributor.authorEPSTEIN, JA
dc.contributor.authorVERZIJL, H
dc.date.accessioned2021-03-03T17:52:22Z
dc.date.available2021-03-03T17:52:22Z
dc.identifier.citationTOMAS-ROCA L., TSAALBI-SHTYLIK A., JANSEN J., SINGH M., EPSTEIN J., Altunoglu U., VERZIJL H., SORIA L., van B., ROSCIOLI T., et al., "De novo mutations in PLXND1 and REV3L cause Möbius syndrome.", Nature communications, cilt.6, ss.7199, 2015
dc.identifier.issn2041-1723
dc.identifier.othervv_1032021
dc.identifier.otherav_4bedb2b0-cf60-49b8-96e4-5211c08acc3e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/54440
dc.identifier.urihttps://doi.org/10.1038/ncomms8199
dc.language.isoeng
dc.titleDe novo mutations in PLXND1 and REV3L cause Möbius syndrome.
dc.typeMakale
dc.relation.journalNature communications
dc.contributor.department, ,
dc.identifier.volume6
dc.identifier.startpage7199
dc.identifier.endpage7199
dc.contributor.firstauthorID182068


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