Publication: Locus heterogeneity and novel TSHR mutations in consanguineous families with congenital non-goitrous hypothyroidism
dc.contributor.author | Cangül, Hakan | |
dc.contributor.author | Aycan, Zehra | |
dc.contributor.author | Morgan, Neil | |
dc.contributor.author | Forman, Julia | |
dc.contributor.author | Çetinkaya, Semra | |
dc.contributor.author | Baş, Veysel | |
dc.contributor.author | Demir, Korcan | |
dc.contributor.author | Yuca, Sevil Arı | |
dc.contributor.author | Kirby, Gail | |
dc.contributor.author | Pasha, Shanaz | |
dc.contributor.author | Kendall, Michaela | |
dc.contributor.author | Hoegler, Wolfgang | |
dc.contributor.author | Barret, T. G. | |
dc.contributor.author | Maher, E. R. | |
dc.contributor.buuauthor | Sağlam, Halil | |
dc.contributor.buuauthor | Yakut, Tahsin | |
dc.contributor.buuauthor | Gülten, Tuna | |
dc.contributor.buuauthor | Karkucak, Mutlu | |
dc.contributor.buuauthor | Eren, Erdal | |
dc.contributor.department | Tıp Fakültesi | |
dc.contributor.department | Tıp Fakültesi | |
dc.contributor.department | Tıbbi Genetik Ana Bilim Dalı | |
dc.contributor.department | Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı | |
dc.contributor.orcid | 0000-0003-0710-5422 | |
dc.contributor.orcid | 0000-0002-1684-1053 | |
dc.contributor.researcherid | C-7392-2019 | |
dc.contributor.researcherid | AAM-1734-2020 | |
dc.date.accessioned | 2022-08-17T06:18:06Z | |
dc.date.available | 2022-08-17T06:18:06Z | |
dc.date.issued | 2010-09 | |
dc.description | Bu çalışma, 06-08 Eylül 2010 tarihleri arasında Warwick[İngiltere]’da düzenlenen British Human Genetics Conference’da bildiri olarak sunulmuştur. | |
dc.identifier.citation | Cangül, H. vd. (2010). "Locus heterogeneity and novel TSHR mutations in consanguineous families with congenital non-goitrous hypothyroidism". Journal of Medical Genetics, 47(Supplement 1), S59-S59. | |
dc.identifier.endpage | 59 | |
dc.identifier.issn | 0022-2593 | |
dc.identifier.startpage | 59 | |
dc.identifier.uri | http://hdl.handle.net/11452/28217 | |
dc.identifier.volume | 47, Supplement 1 | |
dc.identifier.wos | 000283762600115 | |
dc.indexed.wos | SCIE | |
dc.indexed.wos | CPCIS | |
dc.language.iso | en | |
dc.publisher | BMJ Publing Group | |
dc.relation.collaboration | Yurt içi | |
dc.relation.collaboration | Yurt dışı | |
dc.relation.collaboration | Sanayi | |
dc.relation.journal | Journal of Medical Genetics | |
dc.relation.publicationcategory | Konferans Öğesi - Uluslararası | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Genetics & heredity | |
dc.subject.wos | Genetics & heredity | |
dc.title | Locus heterogeneity and novel TSHR mutations in consanguineous families with congenital non-goitrous hypothyroidism | |
dc.type | Meeting Abstract | |
dc.wos.quartile | Q1 | |
dspace.entity.type | Publication | |
local.contributor.department | Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı | |
local.contributor.department | Tıp Fakültesi/Tıbbi Genetik Ana Bilim Dalı | |
local.indexed.at | WOS |
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