HuGE Literature Finder
Records 1-8
Pathological Effects of the FMR1 CGG-Repeat Polymorphism (5-55 Repeat Numbers): Systematic Review and Meta-Analysis.
The Tohoku journal of experimental medicine 2016 05 239 (1): 57-66. Yang Wenjing, Fan Cuihua, Chen Liangyuan, Cui Zhaolei, Bai Ye, Lan Fengh |
Low-normal FMR1 CGG repeat length: phenotypic associations.
Frontiers in genetics 2014 5 309. Mailick Marsha R, Hong Jinkuk, Rathouz Paul, Baker Mei W, Greenberg Jan S, Smith Leann, Maenner Matth |
Intermediate FMR1 alleles and cognitive and/or behavioural phenotypes.
European journal of human genetics : EJHG 2011 Aug 19 (8): 921-3. Madrigal Irene, Xunclà Mar, Tejada Maria Isabel, Martínez Francisco, Fernández-Carvajal Isabel, Pérez-Jurado Luís Alberto, Rodriguez-Revenga Laia, Milà Montserr |
Co-occurring diagnoses among FMR1 premutation allele carriers.
Clinical genetics 2010 Apr 77 (4): 374-81. Hunter J E, Rohr J K, Sherman S |
No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50.
American journal of human genetics 2008 Dec 83 (6): 692-702. Hunter Jessica Ezzell, Allen Emily Graves, Abramowitz Ann, Rusin Michele, Leslie Mary, Novak Gloria, Hamilton Debra, Shubeck Lisa, Charen Krista, Sherman Stephanie |
Impact of the Fragile X mental retardation 1 (FMR1) gene premutation on neuropsychiatric functioning in adult males without fragile X-associated Tremor/Ataxia syndrome: a controlled study.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Sep 147B (6): 859-72. Kogan Cary S, Turk Jeremy, Hagerman Randi J, Cornish Kim |
Age-dependent cognitive changes in carriers of the fragile X syndrome.
Cortex; a journal devoted to the study of the nervous system and behavior 2008 Jun 44 (6): 628-36. Cornish Kim M, Li Lexin, Kogan Cary S, Jacquemont Sebastien, Turk Jeremy, Dalton Ann, Hagerman Randi J, Hagerman Paul |
Distribution of CGG repeats and FRAXAC1/DXS548 alleles in South American populations.
American journal of medical genetics 2002 Aug 111 (3): 243-52. Mingroni-Netto Regina Célia, Angeli Claudia B, Auricchio Maria Teresa B M, Leal-Mesquita Emygdia R, Ribeiro-dos-Santos Andrea K C, Ferrari Iris, Hutz Mara H, Salzano Francisco M, Hill Kim, Hurtado A Magdalena, Vianna-Morgante Angela |
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- Page last updated:Jan 19, 2021
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