Show simple item record

dc.contributor.authorSM, WEITZER
dc.contributor.authorENDER, KARACA
dc.contributor.authorPEHLİVAN, DAVUT
dc.contributor.authorTA, HAREL
dc.contributor.authorHM, SHIRAISHI
dc.contributor.authorYEŞİL, GÖZDE
dc.contributor.authorNU, JHANGIANI
dc.contributor.authorWISZNIEWSKI, WA
dc.contributor.authorBAYRAM, YAVUZ
dc.contributor.authorGAMBIN, THOMAS
dc.date.accessioned2019-10-05T21:37:20Z
dc.date.available2019-10-05T21:37:20Z
dc.date.issued2014-10-22
dc.identifier.urihttps://hdl.handle.net/20.500.12645/7781
dc.language.isoen
dc.subjectENDER K., PEHLİVAN D., TA H., SM W., HM S., GAMBIN T., BAYRAM Y., WISZNIEWSKI W., NU J., YEŞİL G., -Genomic Sequencing Approaches Indentifies Novel Rare Variants in Patients with Mendelian Neurologic Disease-, american society of human genetics, 18 - 22 October 2014
dc.titleGenomic Sequencing Approaches Indentifies Novel Rare Variants in Patients with Mendelian Neurologic Disease
dc.typeConference Paper
local.avesis.response7657


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record