Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Fragile X Syndrome and MAOA[original query] |
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| Brief report: aggression and stereotypic behavior in males with fragile X syndrome--moderating secondary genes in a "single gene" disorder. Journal of autism and developmental disorders 2008 Jan 38 (1): 184-9. Hessl David, Tassone Flora, Cordeiro Lisa, Koldewyn Kami, McCormick Carolyn, Green Cherie, Wegelin Jacob, Yuhas Jennifer, Hagerman Randi |
| Testing for association of the monoamine oxidase A promoter polymorphism with brain structure volumes in both autism and the fragile X syndrome. Journal of neurodevelopmental disorders 2014 6 (1): 6. Wassink Thomas H, Hazlett Heather C, Davis Lea K, Reiss Allan L, Piven Jose |
| Molecular biomarkers predictive of sertraline treatment response in young children with fragile X syndrome. Brain & development 2017 Feb . AlOlaby Reem Rafik, Sweha Stefan R, Silva Marisol, Durbin-Johnson Blythe, Yrigollen Carolyn M, Pretto Dalyir, Hagerman Randi J, Tassone Flo |
| Genetic modifiers in rare disorders: the case of fragile X syndrome. European journal of human genetics : EJHG 2020 8 29 (1): 173-183. Crawford Hayley, Scerif Gaia, Wilde Lucy, Beggs Andrew, Stockton Joanne, Sandhu Pria, Shelley Lauren, Oliver Chris, McCleery Jose |
- Page last reviewed:Feb 1, 2024
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