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Exome sequencing reveals novel candidate variants for endometriosis and endometrial serous adenocarcinoma in a single family having multiple affected members

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dc.contributor.authorKina, B. G.
dc.contributor.authorSelcuki, N. F. Topbas
dc.contributor.authorBahat, P. Yalcin
dc.contributor.authorUsta, T.
dc.contributor.authorTuncer, F. N.
dc.contributor.authorOral, E.
dc.date.accessioned2022-10-18T20:59:16Z
dc.date.available2022-10-18T20:59:16Z
dc.date.issued2022-07-01T00:00:00Z
dc.identifier.citationKina B. G. , Selcuki N. F. T. , Bahat P. Y. , Usta T., Tuncer F. N. , Oral E., -Exome sequencing reveals novel candidate variants for endometriosis and endometrial serous adenocarcinoma in a single family having multiple affected members-, HUMAN REPRODUCTION, cilt.37, 2022
dc.identifier.urihttp://hdl.handle.net/20.500.12645/31144
dc.identifier.wosWOS:000840076003094
dc.titleExome sequencing reveals novel candidate variants for endometriosis and endometrial serous adenocarcinoma in a single family having multiple affected members
dc.typeArticle
dspace.entity.typePublication
local.avesis.idf6b58d0a-0ab8-4b0c-9a9a-83db3f7b01c3
local.publication.isinternational1

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