X‐Linked Intellectual Disability Genetics
Author:
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/9780470015902.a0006175.pub2
Reference61 articles.
1. X-linked mental retardation with variable stature, head circumference, and testicular volume linked to Xq12-q21
2. X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28
3. Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia
4. ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation
5. A gene for FG syndrome maps in the Xq12-q21.31 region
Cited by 2 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. X-Linked CNV in Pathogenetics of Intellectual Disability;Russian Journal of Genetics;2022-10
2. Severe neurocognitive and growth disorders due to variation in THOC2 , an essential component of nuclear mRNA export machinery;Human Mutation;2018-06-14
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