Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Atrophy and FMR1[original query] |
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| Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort. Neurology 2004 Jul 63 (2): 362-3. Tan E K, Zhao Y, Puong K Y, Law H Y, Chan L L, Yew K, Tan C, Shen H, Chandran V R, Teoh M L, Yih Y, Pavanni R, Wong M C, Ng I |
| Fragile X gene premutation in multiple system atrophy. Journal of the neurological sciences 2004 Dec 227 (1): 115-8. Garland E M, Vnencak-Jones C L, Biaggioni I, Davis T L, Montine T J, Robertson |
| FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy. Archives of neurology 2005 Jun 62 (6): 962-6. Biancalana Valérie, Toft Mathias, Le Ber Isabelle, Tison François, Scherrer Elisabeth, Thibodeau Stephen, Mandel Jean Louis, Brice Alexis, Farrer Matthew J, Dürr Alexand |
| Screening for FXTAS in 95 Spanish patients negative for Huntington disease. Genetic testing 2008 Mar 12 (1): 135-8. Rodriguez-Revenga Laia, Santos M Mònica, Sánchez Aurora, Pujol Montserrat, Gómez-Anson Beatriz, Badenas Celia, Jiménez Dolores, Madrigal Irene, Milà Montserr |
| Tremor-Ataxia syndrome and primary ovarian insufficiency in an null premutation carrier. Colombia medica (Cali, Colombia) 2018 1 48 (3): 148-151. Saldarriaga-Gil Wilmar, Rodriguez-Guerrero Tatiana, Fandiño-Losada Andres, Ramirez-Cheyne Juli |
| Genetic counseling and carrier screening in candidates for gamete donation at a Portuguese center. JBRA assisted reproduction 2022 8 . Soares Célia Azevedo, Tkachenko Natália, Vale-Fernandes Emídio, Barreiro Márcia, Abreu Maria, Reis Cláudia Falcão, Soares Gabriela, Fortuna Ana Maria, Soares Ana Ri |
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