The clinical significance of fragile sites on human chromosomes
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2000.580301.x/fullpdf
Reference27 articles.
1. Hagerman RJ, Cronister A (Eds) Fragile X syndrome, Diagnosis Treatment and Research, 2nd Ed, John Hopkin's University Press, 1996.
2. Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study - preliminary data;Allingham-Hawkins;Am J Med Genet,1999
3. Elevated levels of FMR1 mRNA in carrier males: A new mechanism of involvement in the Fragile-X syndrome;Tassone;Am J Hum Genet,2000
4. Translational suppression by trinucleotide repeat expansion at FMR1;Feng;Science,1995
5. Imprinting effect in premature ovarian failure combined to paternally inherited fragile X premutations;Hundscheid;Am J Hum Genet,2000
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