Author:
Rifé M.,Badenas C.,Quintó Ll.,Puigoriol E.,Tazón B.,Rodriguez-Revenga L.,Jiménez L.,Sánchez A.,Milà M.
Publisher
Oxford University Press (OUP)
Subject
Cell Biology,Developmental Biology,Obstetrics and Gynaecology,Genetics,Molecular Biology,Embryology,Reproductive Medicine
Reference11 articles.
1. Ashley-Koch AE, Robinson H, Glicksman AE, Nolin SL, Schwartz CE, Brown WT, Turner G and Sherman SL (1998) Examination of factors associated with instability of the FMR1 CGG repeat. Am J Hum Genet63, 776–785.
2. Fu YH, Kuhl DP, Pizzuti A, Pieretti M, Sutcliffe JS, Richards S, Verkerk AJ, Holden JJ, Fenwick RG Jr and Warren ST (1991) Variation of the CGG repeat at the Fragile X site results in genetic instability: resolution of the Sherman paradox. Cell67, 1047–1058.
3. Loesch DZ, Huggins R, Petrovic V and Slater H (1995) Expansion of the CGG repeat in Fragile X in the FMR1 gene depends on the sex of the offspring. Am J Hum Genet57, 1408–1413.
4. Milà M, Castellví-bel S, Sánchez A, Lázaro C, Villa M and Estivill X (1996) Mosaicism for the Fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene. J Med Genet33, 338–340.
5. Milà M, Castellví-Bel S, Giné R, Vázquez C, Badenas C, Sánchez A and Estivill X (1996) A female compound heterozygote (pre- and full mutation) for the CGG FMR1 expansion. Hum Genet98, 419–421.
Cited by
22 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献