自闭症谱系障碍
基因复制
神经认知
表型
遗传咨询
基因型
基因型-表型区分
背景(考古学)
语音延迟
临床意义
自闭症
遗传学
医学
智力残疾
生物信息学
生物
内科学
精神科
基因
认知
古生物学
作者
Laïla El Khattabi,Solveig Heide,Jean‐Hubert Caberg,Joris Andrieux,Martine Doco Fenzy,Caroline Vincent-Delorme,Patrick Callier,Sandra Chantot‐Bastaraud,Alexandra Afenjar,Odile Boute‐Bénéjean,Marie Pierre Cordier,Laurence Faivre,Christine Francannet,Marion Gérard,Alice Goldenberg,Alice Masurel‐Paulet,Anne‐Laure Mosca‐Boidron,Nathalie Marle,Anne Moncla,Nathalie Le Meur
标识
DOI:10.1136/jmedgenet-2018-105389
摘要
Our study shows that 16p13.11 microduplications are likely pathogenic when detected in the context of DD/ID/ASD and supports an essential role of NDE1 and miR-484 in the neurocognitive phenotype. Moreover, it suggests the need for cardiac evaluation and follow-up and a large study to evaluate the aortic disease risk.
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