scholarly article | Q13442814 |
review article | Q7318358 |
P356 | DOI | 10.1159/000091656 |
P698 | PubMed publication ID | 16493202 |
P2093 | author name string | Hall DA | |
Hagerman PJ | |||
Hagerman RJ | |||
Leehey MA | |||
Jacquemont S | |||
P2860 | cites work | Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. | Q46666276 |
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia. | Q50282467 | ||
Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort | Q50283132 | ||
P433 | issue | 3 | |
P921 | main subject | systematic review | Q1504425 |
P304 | page(s) | 151-155 | |
P577 | publication date | 2006-02-21 | |
P1433 | published in | Neuroepidemiology | Q15764043 |
P1476 | title | Prevalence of FMR1 repeat expansions in movement disorders. A systematic review | |
P478 | volume | 26 |
Q24632814 | Advances in the treatment of fragile X syndrome |
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Q34046162 | Identification of expanded alleles of the FMR1 gene among high-risk population in Indonesia by using blood spot screening |
Q33728963 | In the Gray Zone in the Fragile X Gene: What are the Key Unanswered Clinical and Biological Questions? |
Q37199782 | Parkinsonism in FMR1 premutation carriers may be indistinguishable from Parkinson disease |
Q38641503 | Public Health Literature Review of Fragile X Syndrome |
Q46702599 | Recommendations from multi-disciplinary focus groups on cascade testing and genetic counseling for fragile X-associated disorders |
Q47923533 | Screening for intermediate CGG alleles of FMR1 gene in male Iranian patients with Parkinsonism. |
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