FG syndrome: Linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3]
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference25 articles.
1. The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability
2. Localization of two X-linked mental retardation (XLMR) genes to Xp: MRX37 gene at Xp22.31-p22.32 and a putative MRX gene on Xp22.11-p22.2
3. A Novel Murine PKA-Related Protein Kinase Involved in Neuronal Differentiation
4. Deficient long-term memory in mice with a targeted mutation of the cAMP-responsive element-binding protein
5. A gene for FG syndrome maps in the Xq12-q21.31 region
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3. A male infant with Xq22.2q22.3 duplication containingPLP1andMID2;Molecular Genetics & Genomic Medicine;2020-01-17
4. Genetics of X-Linked Intellectual Disability;Neuronal and Synaptic Dysfunction in Autism Spectrum Disorder and Intellectual Disability;2016
5. X‐Linked Intellectual Disability Genetics;eLS;2015-10-15
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