Basit öğe kaydını göster

A de novo complex chromosomal rearrangement involving chromosomes 2, 8 and 13 in a dysmorphic case with polysyndactyly

dc.contributor.authorRosti, Rasim Ozgur
dc.contributor.authorKaraman, Birsen
dc.contributor.authorKayserili, Huelya
dc.contributor.authorOzturk, Havva
dc.contributor.authorBasaran, Seher
dc.contributor.authorYilmaz, Kader
dc.date.accessioned2021-03-05T10:12:34Z
dc.date.available2021-03-05T10:12:34Z
dc.date.issued2009
dc.identifier.citationKaraman B., Rosti R. O. , Yilmaz K., Ozturk H., Kayserili H., Basaran S., "A de novo complex chromosomal rearrangement involving chromosomes 2, 8 and 13 in a dysmorphic case with polysyndactyly", TURKISH JOURNAL OF PEDIATRICS, cilt.51, ss.613-616, 2009
dc.identifier.issn0041-4301
dc.identifier.otherav_a1f33a20-aec5-4fcf-bd6a-9128f4098a0e
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/108485
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/20196399
dc.description.abstractWe report herein a case with dysmorphic features, polysyndactyly and psychomotor mental retardation, who had an apparently balanced de novo translocation between chromosomes 8 and 13 as well as a de novo insertion within chromosome 2 itself.
dc.language.isoeng
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleA de novo complex chromosomal rearrangement involving chromosomes 2, 8 and 13 in a dysmorphic case with polysyndactyly
dc.typeMakale
dc.relation.journalTURKISH JOURNAL OF PEDIATRICS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume51
dc.identifier.issue6
dc.identifier.startpage613
dc.identifier.endpage616
dc.contributor.firstauthorID12634


Bu öğenin dosyaları:

DosyalarBoyutBiçimGöster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster