Correlation betweenFMR1expression and clinical phenotype in discordant dichorionic–diamniotic monozygotic twin sisters with the fragile x mutation
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Reference19 articles.
1. Fragile X and autism: intertwined at the molecular level leading to targeted treatments;Hagerman;Mol Autism,2010
2. New perspectives on the biology of fragile X syndrome;Wang;Curr Opin Genet Dev,2012
3. Genetic counseling and testing for FMR1 gene mutations: practice guidelines of the National Society of Genetic Counselors;Finucane;J Genet Couns,2012
4. Molecular predictors of cognitive involvement in female carriers of fragile X syndrome;Taylor;JAMA,1994
5. What monozygotic twins discordant for phenotype illustrate about mechanisms influencing genetic forms of neurodegeneration;Ketelaar;Clin Genet,2012
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2. Genetics and epigenetics differences in monozygotic twins: the vision of the geneticist;Developmental and Fetal Origins of Differences in Monozygotic Twins;2020
3. Non-coding RNA in Fragile X Syndrome and Converging Mechanisms Shared by Related Disorders;Frontiers in Genetics;2019-03-01
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5. Neurodevelopmental Disorders;Diseases of the Nervous System;2015
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