Publication:
Imerslund-Gräsbeck syndrome: New mutation in amnionless

Simple item page
dc.contributor.authorNarumon Densupsoontornen_US
dc.contributor.authorKleebsabai Sanpakiten_US
dc.contributor.authorChodchanok Vijarnsornen_US
dc.contributor.authorAniruth Pattaragarnen_US
dc.contributor.authorChannagarn Kangwanpornsirien_US
dc.contributor.authorCharnnarong Jatutipsompolen_US
dc.contributor.authorHathaichanok Tirapongpornen_US
dc.contributor.authorPipop Jirapinyoen_US
dc.contributor.authorNidhi P. Shahen_US
dc.contributor.authorAmy C. Sturmen_US
dc.contributor.authorStephan M. Tanneren_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherHuman Cancer Geneticsen_US
dc.contributor.otherOhio State Universityen_US
dc.date.accessioned2018-06-11T05:10:17Z
dc.date.available2018-06-11T05:10:17Z
dc.date.issued2012-06-01en_US
dc.identifier.citationPediatrics International. Vol.54, No.3 (2012)en_US
dc.identifier.doi10.1111/j.1442-200X.2011.03482.xen_US
dc.identifier.issn1442200Xen_US
dc.identifier.issn13288067en_US
dc.identifier.other2-s2.0-84861600481en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/14785
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84861600481&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleImerslund-Gräsbeck syndrome: New mutation in amnionlessen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84861600481&origin=inwarden_US

Files

Collections

Scopus 2011-2015