Basit öğe kaydını göster

Fraser syndrome due to mutations in GRIP1--clinical phenotype in two families and expansion of the mutation spectrum.

dc.contributor.authorSCHANZE, D
dc.contributor.authorAltunoglu, UMUT
dc.contributor.authorKAYSERILI, H
dc.contributor.authorSATKıN, BN
dc.contributor.authorZENKER, M
dc.date.accessioned2021-03-03T17:02:44Z
dc.date.available2021-03-03T17:02:44Z
dc.identifier.citationSCHANZE D., KAYSERILI H., SATKıN B., Altunoglu U., ZENKER M., "Fraser syndrome due to mutations in GRIP1--clinical phenotype in two families and expansion of the mutation spectrum.", American journal of medical genetics. Part A, ss.837-40, 2014
dc.identifier.issn1552-4825
dc.identifier.othervv_1032021
dc.identifier.otherav_47a130d9-6fa5-40e1-b2e4-532dbf61719d
dc.identifier.urihttp://hdl.handle.net/20.500.12627/51678
dc.identifier.urihttps://doi.org/10.1002/ajmg.a.36343
dc.language.isoeng
dc.titleFraser syndrome due to mutations in GRIP1--clinical phenotype in two families and expansion of the mutation spectrum.
dc.typeMakale
dc.relation.journalAmerican journal of medical genetics. Part A
dc.contributor.department, ,
dc.identifier.startpage837
dc.identifier.endpage40
dc.contributor.firstauthorID182033


Bu öğenin dosyaları:

DosyalarBoyutBiçimGöster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster