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A Private 16q24.2q24.3 Microduplication in a Boy with Intellectual Disability, Speech Delay and Mild Dysmorphic Features

机译：私人16Q24.2Q24.3微型综合杂货，具有智力残疾，语音延迟和轻度疑难解定特征

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Orazio Palumbo; Pietro Palumbo; Ester Di Muro; Luigia Cinque; Antonio Petracca; Massimo Carella; Marco Castori;
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1. 16q24.3 Microduplication in a Patient With Developmental Delay, Intellectual Disability, Short Stature, and Nonspecific Dysmorphic Features: Case Report and Review of the Literature [J] . Simona Bucerzan, Diana Miclea, Cecilia Lazea, Frontiers in Pediatrics . 2020,第a期

机译：16Q24.3患者的微统计学，具有发育延迟，智力残疾，身材矮小和非特异性疑风特征：病例报告和文献审查
2. 16q24.3 Microduplication in a Patient With Developmental Delay, Intellectual Disability, Short Stature, and Nonspecific Dysmorphic Features: Case Report and Review of the Literature [J] . Bucerzan Simona, Miclea Diana, Lazea Cecilia, Frontiers in Pediatrics . 2020,第3期

机译：16Q24.3患者中的微量综合症，具有发育延迟，智力残疾，矮小和非特异性疑风特征：案例报告和文献审查
3. Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay [J] . Abdulaziz Asiri, Essra Aloyouni, Muhammad Umair, Annals of Clinical and Translational Neurology . 2020,第6期

机译：突变的RAP1GDS1导致疑难垂特征的新综合征，智力残疾和言语延迟
4. The Use of Lotto Baca in Improving Speech for Children with Intellectual Disability: Single Subject Research Study in Children with Intellectual Disability in Pandita Kindergarten Serang City [C] . Silvi Sundari, Febriani Agung, Wilda Famy, International Conference on Special Education . 2019

机译：乐透培根在提高智力残疾儿童演讲中的使用：帕尔塔幼儿园智能城智力患儿的单一主题研究研究
5. Comparing the Stanford-Binet Intelligence Scale: Fourth Edition and the Wechsler Intelligence Scale for Children-Third Edition in specific learning disability and mild intellectual disability students. [D] . Scott, Lee Ann. 1998

机译：比较针对特定学习障碍者和轻度智力障碍学生的斯坦福－比内特智力量表：第四版和韦氏儿童智力量表（第三版）。
6. A Private 16q24.2q24.3 Microduplication in a Boy with Intellectual Disability Speech Delay and Mild Dysmorphic Features [O] . Orazio Palumbo, Pietro Palumbo, Ester Di Muro, 2020

机译：私人的16q24.2q24.3微复制在有智力残疾言语延迟和轻度畸形特征的男孩中
7. Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features [O] . Jing Zhang, Tomasz Gambin, Bo Yuan, 2017

机译：错误至：E3泛素蛋白蛋白连接酶基因TREP12的HAPLOUSUBUCKE引起智力残疾或没有自闭症谱系障碍，语音延迟和疑难解定特征

A Private 16q24.2q24.3 Microduplication in a Boy with Intellectual Disability, Speech Delay and Mild Dysmorphic Features

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