Concepedia

Fragile X syndrome without CCG amplification has an FMR1 deletion

Ági K. Gedeon, Emma K. Baker, Harriet L. Robinson, M. W. Partington, Bella Gross, Antonella Manca, Bernhard Korn, Annemarie Poustka, S. Yu, G.R. Sutherland,

Nature Genetics · 1992 · 218 citations · 18 references

DOI

Concepts

References

18

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Annemieke J.M.H. Verkerk, Maura Pieretti, James S. Sutcliffe et al. · Cell · 1991 · 3.5K citations

, , +12

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

Ying‐Hui Fu, Derek P.A. Kuhl, Antonio Pizzuti et al. · Cell · 1991 · 2.1K citations

, , +8

Localization of the X inactivation centre on the human X chromosome in Xq13

Carolyn J. Brown, Ronald G. Lafrenière, Vicki E. C. Powers et al. · Nature · 1991 · 382 citations

, , +13

Fragile Sites on Human Chromosomes

Journal of Medical Genetics · 1986 · 243 citations · Full text

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Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.

Robert I. Richards, K. Holman, H.M. Kozman et al. · Journal of Medical Genetics · 1991 · 138 citations · Full text

, , +16