Concepedia

Molecular analysis of mutations in the gene FMR-1 segregating in fragile X families

Peter Steinbach, Doris W�hrle, Gholamali Tariverdian, Ingo Kennerknecht, Gotthold Barbi, H. Edlinger, H. Enders, M. G�tz-Sothmann, H. Heilbronner, D. Hosenfeld,

Human Genetics · 1993 · 18 citations · 39 references

DOI

Concepts

References

39

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

Andrew P. Feinberg, Bert Vogelstein · Analytical Biochemistry · 1983 · 25.2K citations

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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

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Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome

I. Oberlé, F. Rousseau, Dominique Heitz et al. · Science · 1991 · 1.5K citations

, , +16

Absence of expression of the FMR-1 gene in fragile X syndrome

Maura Pieretti, Ying‐Hui Fu, Stephen T. Warren et al. · Cell · 1991 · 1.5K citations

, , +11