Advances in X-linked mental retardation
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Pediatrics, Perinatology and Child Health
Reference27 articles.
1. Genetic syndromes among individuals with mental retardation
2. Monogenic X-linked mental retardation: Is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations
3. Clinical and molecular contributions to the understanding of X-linked mental retardation
4. Nonsyndromic X-linked mental retardation: where are the missing mutations?
5. Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 (MCT8) Gene
Cited by 17 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Mental Retardation and Isoleucine Metabolism;Branched Chain Amino Acids in Clinical Nutrition;2015
2. Loss-of-function mutation of collybistin is responsible for X-linked mental retardation associated with epilepsy;Journal of Human Genetics;2011-06-02
3. Genetics of Early Onset Cognitive Impairment;Annual Review of Genomics and Human Genetics;2010-09-01
4. Identification of ectodysplasin-A receptor gene deletion at 2q12.2 and a potential autosomal MR locus;European Journal of Human Genetics;2008-10-15
5. Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia;Journal of Medical Genetics;2008-07-08
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