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dc.contributor.authorApak, Memnune
dc.contributor.authorIşık, U
dc.contributor.authorDehgan, Tahir
dc.contributor.authorBAŞARAN, Seher
dc.date.accessioned2021-03-02T20:08:13Z
dc.date.available2021-03-02T20:08:13Z
dc.date.issued2008
dc.identifier.citationIşık U., BAŞARAN S., Dehgan T., Apak M., "Corpus callosum agenesis in trisomy 8p11.23 and monosomy 4q34 because of maternal translocation", PEDIATRIC NEUROLOGY, cilt.39, sa.1, ss.55-57, 2008
dc.identifier.issn0887-8994
dc.identifier.othervv_1032021
dc.identifier.otherav_0071ddf7-55f7-47b6-9a3f-72856c75aa88
dc.identifier.urihttp://hdl.handle.net/20.500.12627/6289
dc.identifier.urihttps://doi.org/10.1016/j.pediatrneurol.2008.03.012
dc.description.abstractWe report on a 3-year-old boy with partial trisomy 8 p11.23 -> pter and partial monosomy 4q34 -> qter, associated with developmental delay, complete agenesis of the corpus callosum, and mild dysmorphic features. Although agenesis of the corpus callosum is not a rare finding among chromosomal abnormalities, partial trisomy 8p together with partial monosomy 4q, resulting from a maternal translocation, was not previously reported, to the best of our knowledge. (C) 2008 by Elsevier Inc. All rights reserved.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp (MED)
dc.subjectPEDİATRİ
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectNöroloji
dc.titleCorpus callosum agenesis in trisomy 8p11.23 and monosomy 4q34 because of maternal translocation
dc.typeMakale
dc.relation.journalPEDIATRIC NEUROLOGY
dc.contributor.departmentPremed Prenatal Diagnosis & Genetic Diseases Center , ,
dc.identifier.volume39
dc.identifier.issue1
dc.identifier.startpage55
dc.identifier.endpage57
dc.contributor.firstauthorID727026


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