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Decoding 51 Thousand Individuals for the HFE Gene Mutations and Analyzing Cancer Risk in the Most Common Genetic Disorder, Hereditary Hemochromatosis

dc.contributor.authorBaras, A.
dc.contributor.authorCorbali, M. O.
dc.contributor.authorWilliams, M. S.
dc.contributor.authorOverton, J.
dc.contributor.authorKip, N. S.
dc.contributor.authorMetpally, R.
dc.contributor.authorWilliams, H.
dc.contributor.authorMcDonnell, J.
dc.contributor.authorKrishnamurthy, S.
dc.contributor.authorHarrison, H.
dc.contributor.authorCarey, D. J.
dc.date.accessioned2021-03-04T17:54:08Z
dc.date.available2021-03-04T17:54:08Z
dc.identifier.citationCorbali M. O. , Metpally R., Williams H., McDonnell J., Krishnamurthy S., Harrison H., Carey D. J. , Williams M. S. , Baras A., Overton J., et al., "Decoding 51 Thousand Individuals for the HFE Gene Mutations and Analyzing Cancer Risk in the Most Common Genetic Disorder, Hereditary Hemochromatosis", Meeting of the Association-for-Molecular-Pathology, Charlottetown, Kanada, 10 - 12 Kasım 2016, cilt.18, ss.940
dc.identifier.othervv_1032021
dc.identifier.otherav_87dc95aa-c74f-4c62-921e-2fa00289c0bb
dc.identifier.urihttp://hdl.handle.net/20.500.12627/92242
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectCerrahi Tıp Bilimleri
dc.subjectPatoloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectBiyoloji ve Biyokimya
dc.subjectPATOLOJİ
dc.subjectTıp
dc.titleDecoding 51 Thousand Individuals for the HFE Gene Mutations and Analyzing Cancer Risk in the Most Common Genetic Disorder, Hereditary Hemochromatosis
dc.typeBildiri
dc.contributor.departmentGeisinger Health System , ,
dc.identifier.volume18
dc.contributor.firstauthorID150392


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