Novel FGF10 mutation in autosomal dominant aplasia of lacrimal and salivary glands.

dc.contributor.author	Kim, JW
dc.contributor.author	DEDEOGLU, Selin Ece
dc.contributor.author	Kim, YJ
dc.contributor.author	Seymen, Figen
dc.contributor.author	KORUYUCU, Mine
dc.contributor.author	TOPTANCI, IR
dc.contributor.author	BALSAK, S
dc.contributor.author	CELEPKOLU, T
dc.contributor.author	Shin, TJ
dc.contributor.author	Hyun, HK
dc.date.accessioned	2021-03-04T07:48:15Z
dc.date.available	2021-03-04T07:48:15Z
dc.identifier.citation	Seymen F., KORUYUCU M., TOPTANCI I., BALSAK S., DEDEOGLU S. E. , CELEPKOLU T., Shin T., Hyun H., Kim Y., Kim J., "Novel FGF10 mutation in autosomal dominant aplasia of lacrimal and salivary glands.", Clinical oral investigations, cilt.21, ss.167-172, 2017
dc.identifier.issn	1432-6981
dc.identifier.other	vv_1032021
dc.identifier.other	av_5ff0f527-72d1-4f24-9991-fa347be58dbf
dc.identifier.uri	http://hdl.handle.net/20.500.12627/66993
dc.identifier.uri	https://doi.org/10.1007/s00784-016-1771-x
dc.language.iso	eng
dc.title	Novel FGF10 mutation in autosomal dominant aplasia of lacrimal and salivary glands.
dc.type	Makale
dc.relation.journal	Clinical oral investigations
dc.contributor.department	Dicle Üniversitesi , ,
dc.identifier.volume	21
dc.identifier.startpage	167
dc.identifier.endpage	172
dc.contributor.firstauthorID	159028

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