6p22.3 deletion: report of a patient with autism, severe intellectual disability and electroencephalographic anomalies.

导出 OA

翻译打印收藏纠错

作者： Daniela,Di Benedetto ^[1] ; Giuseppa,Di Vita ^[2] ; Corrado,Romano ^[3] ; Mariangela Lo,Giudice ^[4] ; Girolamo Aurelio,Vitello ^[2] ; Marinella,Zingale ^[5] ; Lucia,Grillo ^[1] ; Lucia,Castiglia ^[1] ; Sebastiano Antonino,Musumeci ^[2] ; Marco,Fichera ^[1]

作者单位： Laboratory of Medical Genetics, I.R.C.C.S. Associazione Oasi Maria Santissima, Troina, Italy. ^[1] Unit of Neurology, I.R.C.C.S. Associazione Oasi Maria Santissima, Troina, Italy. ^[2] Unit of Pediatrics and Medical Genetics, I.R.C.C.S. Associazione Oasi Maria Santissima, Troina, Italy. ^[3] Unit of Neuromuscular Disease, I.R.C.C.S. Associazione Oasi Maria Santissima, Troina, Italy. ^[4] Unit of Psychology, I.R.C.C.S. Associazione Oasi Maria Santissima, Troina, Italy. ^[5] Medical Genetics, University of Catania, Catania, Italy. ^[6]

DOI 10.1186/1755-8166-6-4

PMID 23324214

发布时间 2022-01-29

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交

浏览53

Molecular cytogenetics

2013年6卷1期

4页

相似文献

中文期刊
外文期刊
学位论文
会议论文

检索历史清除

6p22.3 deletion: report of a patient with autism, severe intellectual disability and electroencephalographic anomalies.

Molecular cytogenetics

相似文献

Molecular cytogenetics

相关期刊

参考文献：
指定格式：	NoteExpress EndNote RefWorks NoteFirst

检索历史 清除

6p22.3 deletion: report of a patient with autism, severe intellectual disability and electroencephalographic anomalies.

Molecular cytogenetics

相似文献

Molecular cytogenetics

相关期刊

检索历史清除