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dc.contributor.authorAtay, Zeynep
dc.contributor.authorAbaci, Ayhan
dc.contributor.authorGulsuner, Hilal Unal
dc.contributor.authorPierce, Sarah B.
dc.contributor.authorGambin, Tomasz
dc.contributor.authorLee, Ming
dc.contributor.authorTuran, Serap
dc.contributor.authorBober, Ece
dc.contributor.authorAtik, Mehmed M.
dc.contributor.authorWalsh, Tom
dc.contributor.authorKaraca, Ender
dc.contributor.authorPehlivan, Davut
dc.contributor.authorJhangiani, Shalini N.
dc.contributor.authorMuzny, Donna
dc.contributor.authorBereket, Abdullah
dc.contributor.authorLupski, James R.
dc.contributor.authorYesil, Gözde
dc.contributor.authorBuyukgebiz, Atilla
dc.contributor.authorBoerwinkle, Eric
dc.contributor.authorGibbs, Richard A.
dc.contributor.authorKing, Mary-Claire
dc.contributor.authorBayram, Yavuz
dc.contributor.authorGulsuner, Suleyman
dc.contributor.authorGuran, Tulay
dc.date.accessioned2021-03-04T12:34:56Z
dc.date.available2021-03-04T12:34:56Z
dc.date.issued2015
dc.identifier.citationBayram Y., Gulsuner S., Guran T., Abaci A., Yesil G., Gulsuner H. U. , Atay Z., Pierce S. B. , Gambin T., Lee M., et al., "Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism", Journal of Clinical Endocrinology and Metabolism, cilt.100, sa.5, 2015
dc.identifier.issn0021-972X
dc.identifier.othervv_1032021
dc.identifier.otherav_77fde6cd-010d-4bbd-920e-b54725ed1960
dc.identifier.urihttp://hdl.handle.net/20.500.12627/82341
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84929359417&origin=inward
dc.identifier.urihttps://doi.org/10.1210/jc.2015-1150
dc.language.isoeng
dc.titleHomozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism
dc.typeMakale
dc.relation.journalJournal of Clinical Endocrinology and Metabolism
dc.contributor.departmentBaylor College of Medicine , ,
dc.identifier.volume100
dc.identifier.issue5
dc.contributor.firstauthorID1042741


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