Author:
Rodriguez-Revenga Laia,Madrigal Irene,Pagonabarraga Javier,Xunclà Mar,Badenas Celia,Kulisevsky Jaime,Gomez Beatriz,Milà Montserrat
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference23 articles.
1. Rife M, Badenas C, Mallolas J et al: Incidence of fragile X in 5000 consecutive newborn males. Genet Test 2003; 7: 339–343.
2. Rousseau F, Rouillard P, Morel ML, Khandjian EW, Morgan K : Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome. Am J Hum Genet 1995; 57: 1006–1018.
3. Dombrowski C, Lévesque S, Morel ML, Rouillard P, Morgan K, Rousseau F : Premutation and intermediate-size FMR1 alleles in 10 572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles. Hum Mol Genet 2002; 11: 371–378.
4. Cronister A, Schreiner R, Wittenberger M, Amiri K, Harris K, Hagerman RJ : Heterozygous fragile X female: historical, physical, cognitive, and cytogenetic features. Am J Med Genet 1991; 38: 269–274.
5. Hagerman RJ, Leehey M, Heinrichs W et al: Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology 2001; 57: 127–130.
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