Show simple item record

Autosomal recessive Robinow syndrome is caused by homozygous mutations in ROR2.

dc.contributor.authorRajab, A
dc.contributor.authorOldridge, M
dc.contributor.authorElanko, N
dc.contributor.authorTernes-Pereira, E
dc.contributor.authorTuysuz, B
dc.contributor.authorMurday, VA
dc.contributor.authorPatton, MA
dc.contributor.authorWilkie, AOM
dc.contributor.authorJeffrey, S
dc.contributor.authorAfzal, AR
dc.contributor.authorFenske, CD
dc.date.accessioned2021-03-05T17:50:11Z
dc.date.available2021-03-05T17:50:11Z
dc.date.issued2000
dc.identifier.citationAfzal A., Rajab A., Fenske C., Oldridge M., Elanko N., Ternes-Pereira E., Tuysuz B., Murday V., Patton M., Wilkie A., et al., "Autosomal recessive Robinow syndrome is caused by homozygous mutations in ROR2.", AMERICAN JOURNAL OF HUMAN GENETICS, cilt.67, ss.389, 2000
dc.identifier.issn0002-9297
dc.identifier.otherav_c7771ffa-c06a-4dc0-9b17-30b2af2e15e6
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/132221
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.titleAutosomal recessive Robinow syndrome is caused by homozygous mutations in ROR2.
dc.typeMakale
dc.relation.journalAMERICAN JOURNAL OF HUMAN GENETICS
dc.contributor.department, ,
dc.identifier.volume67
dc.identifier.issue4
dc.identifier.startpage389
dc.identifier.endpage389
dc.contributor.firstauthorID126639


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