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Holt-Oram syndrome because of the novel TBX5 mutation c.481A>C.

dc.contributor.authorKAYSERILI, H
dc.contributor.authorALTUNOĞLU, UMUT
dc.contributor.authorToksoy, Güven
dc.contributor.authorKoçak, Eker
dc.date.accessioned2021-03-06T11:38:37Z
dc.date.available2021-03-06T11:38:37Z
dc.identifier.citationKoçak E., ALTUNOĞLU U., Toksoy G., KAYSERILI H., "Holt-Oram syndrome because of the novel TBX5 mutation c.481A>C.", Clinical dysmorphology, cilt.25, ss.192-4, 2016
dc.identifier.issn0962-8827
dc.identifier.othervv_1032021
dc.identifier.otherav_f0041bad-5942-4e65-ae2f-e9feb41b71c4
dc.identifier.urihttp://hdl.handle.net/20.500.12627/157527
dc.identifier.urihttps://doi.org/10.1097/mcd.0000000000000121
dc.language.isoeng
dc.titleHolt-Oram syndrome because of the novel TBX5 mutation c.481A>C.
dc.typeMakale
dc.relation.journalClinical dysmorphology
dc.contributor.department, ,
dc.identifier.volume25
dc.identifier.startpage192
dc.identifier.endpage4
dc.contributor.firstauthorID178870


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