Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Angelman Syndrome and MECP2[original query] |
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MECP2 analysis in mentally retarded patients: implications for routine DNA diagnostics. European journal of human genetics : EJHG 2004 Jan 12 (1): 24-8. Kleefstra Tjitske, Yntema Helger G, Nillesen Willy M, Oudakker Astrid R, Mullaart Reinier A, Geerdink Niels, van Bokhoven Hans, de Vries Bert B A, Sistermans Erik A, Hamel Ben C |
MECP2 mutation analysis in patients with mental retardation. American journal of medical genetics. Part A 2005 Jan 132A (2): 121-4. Ylisaukko-Oja Tero, Rehnström Karola, Vanhala Raija, Kempas Elli, von Koskull Harriet, Tengström Carola, Mustonen Aki, Ounap Katrin, Lähdetie Jaana, Järvelä Ir |
Screening for MECP2 mutations in Spanish patients with an unexplained mental retardation. Clinical genetics 2006 Aug 70 (2): 140-4. Tejada M-I, Peñagarikano O, Rodriguez-Revenga L, Martinez-Bouzas C, García B, Bádenas C, Guitart M, Minguez M, García-Alegría E, Sanz-Parra A, Beristain E, Milá |
Genetic diagnoses in pediatric patients with epilepsy and comorbid intellectual disability. Epilepsy research 2021 1 170 106552. Yang Mei, Xu Bocheng, Wang Jiamin, Zhang Zhu, Xie Hanbing, Wang He, Hu Ting, Liu Shanli |
[Diagnostic value of whole exome sequencing for patients with intellectual disability or global developmental delay]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 5 40 (6): 648-654. Yangyan Li, Dongzhu Lei, Caiyun Li, Dongqun Huang, Jufang Tan, Haoqing Zha |
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