Publication: Investigation of apc mutations of a patient with fap and her family members by heterodublex analyses
dc.contributor.author | Menigatti, M | |
dc.contributor.author | Benatti, P | |
dc.contributor.author | Pedroni, M | |
dc.contributor.author | Scarselli, A | |
dc.contributor.author | Borghi, F | |
dc.contributor.author | Sala, E | |
dc.contributor.author | Yerci, O | |
dc.contributor.author | de Leon, MP | |
dc.contributor.buuauthor | TUNCA, BERRİN | |
dc.contributor.buuauthor | Çeçener, Gülşah | |
dc.contributor.buuauthor | YILMAZLAR, AHMET TUNCAY | |
dc.contributor.buuauthor | ÇEÇENER, GÜLŞAH | |
dc.contributor.buuauthor | Yılmazlar, Tuncay | |
dc.contributor.buuauthor | Zorluoglu, A | |
dc.contributor.buuauthor | EGELİ, ÜNAL | |
dc.contributor.buuauthor | Yerci, Ömer | |
dc.contributor.buuauthor | YERCİ, ÖMER | |
dc.contributor.department | Bursa Uludağ Üniversitesi/Tıp Fakültesi/Patoloji Anabilim Dalı. | |
dc.contributor.department | Bursa Uludağ Üniversitesi/Tıp Fakültesi/Genel Cerrahi Anabilim Dalı. | |
dc.contributor.department | Bursa Uludağ Üniversitesi/Tıp Fakültesi/Medikal Biyoloji ve Genetik Anabilim Dalı. | |
dc.contributor.orcid | 0000-0002-1619-6680 | |
dc.contributor.orcid | 0000-0002-3820-424X | |
dc.contributor.orcid | 0000-0001-7904-883X | |
dc.contributor.researcherid | AAH-1420-2021 | |
dc.contributor.researcherid | ABI-6078-2020 | |
dc.date.accessioned | 2024-09-03T06:00:36Z | |
dc.date.available | 2024-09-03T06:00:36Z | |
dc.date.issued | 2002-05-01 | |
dc.description | Bu çalışma, 25-28 Mayıs 2002 tarihleri arasında Strsbourg[Fransa]’da düzenlenen European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics’da bildiri olarak sunulmuştur. | |
dc.description.sponsorship | European Soc Human Genet | |
dc.identifier.endpage | 86 | |
dc.identifier.issn | 1018-4813 | |
dc.identifier.issue | Supplement 1 | |
dc.identifier.startpage | 86 | |
dc.identifier.uri | https://hdl.handle.net/11452/44275 | |
dc.identifier.volume | 10 | |
dc.identifier.wos | 000187166100145 | |
dc.indexed.wos | WOS.ISTP | |
dc.indexed.wos | WOS.SCI | |
dc.language.iso | en | |
dc.publisher | Nature Publishing Group | |
dc.relation.journal | European Journal Of Human Genetics | |
dc.relation.publicationcategory | Konferans Öğesi - Uluslararası | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Science & technology | |
dc.subject | Life sciences & biomedicine | |
dc.subject | Biochemistry & molecular biology | |
dc.subject | Genetics & heredity | |
dc.subject | Biochemistry & molecular biology | |
dc.subject | Genetics & heredity | |
dc.title | Investigation of apc mutations of a patient with fap and her family members by heterodublex analyses | |
dc.type | Meeting Abstract | |
dspace.entity.type | Publication | |
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