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A novel mutation in the <i>TRIP11</i> gene: Diagnostic approach from relatively common skeletal dysplasias to an extremely rare Odontochondrodysplasia.

dc.contributor.authorDilruba Aslanger, Ayca
dc.contributor.authorElcioglu, Nursel H
dc.contributor.authorYesil, Gözde
dc.contributor.authorYeter, Burcu
dc.date.accessioned2021-12-10T10:32:35Z
dc.date.available2021-12-10T10:32:35Z
dc.identifier.citationYeter B., Dilruba Aslanger A., Yesil G., Elcioglu N. H. , "A novel mutation in the <i>TRIP11</i> gene: Diagnostic approach from relatively common skeletal dysplasias to an extremely rare Odontochondrodysplasia.", Journal of clinical research in pediatric endocrinology, 2021
dc.identifier.issn1308-5727
dc.identifier.othervv_1032021
dc.identifier.otherav_46647e49-3dfb-4993-8146-0b772c05c650
dc.identifier.urihttp://hdl.handle.net/20.500.12627/170109
dc.identifier.urihttps://avesis.istanbul.edu.tr/api/publication/46647e49-3dfb-4993-8146-0b772c05c650/file
dc.identifier.urihttps://doi.org/10.4274/jcrpe.galenos.2021.2021.0099
dc.language.isoeng
dc.titleA novel mutation in the <i>TRIP11</i> gene: Diagnostic approach from relatively common skeletal dysplasias to an extremely rare Odontochondrodysplasia.
dc.typeMakale
dc.relation.journalJournal of clinical research in pediatric endocrinology
dc.contributor.department, ,
dc.contributor.firstauthorID2751181


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