Tissue-specific methylation differences and cognitive function in fragile X premutation females
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference24 articles.
1. Molecular-neurobehavioral associations in females with the fragile X full mutation
2. Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group children
3. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
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1. Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease;The Journal of Clinical Endocrinology & Metabolism;2019-05-01
2. FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the FMR1 Gene;Frontiers in Genetics;2018-11-02
3. Health Profiles of Mosaic Versus Non-mosaic FMR1 Premutation Carrier Mothers of Children With Fragile X Syndrome;Frontiers in Genetics;2018-05-16
4. Size and methylation mosaicism in males with Fragile X syndrome;Expert Review of Molecular Diagnostics;2017-10-12
5. The Molecular Biology of Premutation Expanded Alleles;FXTAS, FXPOI, and Other Premutation Disorders;2016
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