dc.contributor.author | Apak, Memnune | |
dc.contributor.author | Işık, U | |
dc.contributor.author | Dehgan, Tahir | |
dc.contributor.author | BAŞARAN, Seher | |
dc.date.accessioned | 2021-03-02T20:08:13Z | |
dc.date.available | 2021-03-02T20:08:13Z | |
dc.date.issued | 2008 | |
dc.identifier.citation | Işık 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.issn | 0887-8994 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_0071ddf7-55f7-47b6-9a3f-72856c75aa88 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/6289 | |
dc.identifier.uri | https://doi.org/10.1016/j.pediatrneurol.2008.03.012 | |
dc.description.abstract | We 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.iso | eng | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Klinik Tıp | |
dc.subject | KLİNİK NEUROLOJİ | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | PEDİATRİ | |
dc.subject | Tıp | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Çocuk Sağlığı ve Hastalıkları | |
dc.subject | Nöroloji | |
dc.title | Corpus callosum agenesis in trisomy 8p11.23 and monosomy 4q34 because of maternal translocation | |
dc.type | Makale | |
dc.relation.journal | PEDIATRIC NEUROLOGY | |
dc.contributor.department | Premed Prenatal Diagnosis & Genetic Diseases Center , , | |
dc.identifier.volume | 39 | |
dc.identifier.issue | 1 | |
dc.identifier.startpage | 55 | |
dc.identifier.endpage | 57 | |
dc.contributor.firstauthorID | 727026 | |