Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox-Reference-Cited by-同舟云学术

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

Published:1991-12 Issue:6 Volume:67 Page:1047-1058
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Fu Ying-Hui,Kuhl Derek P.A.,Pizzuti Antonio,Pieretti Maura,Sutcliffe James S.,Richards Stephen,Verkert Annemieke J.M.H.,Holden Jeanette J.A.,Fenwick Raymond G.,Warren Stephen T.,Oostra Ben A.,Nelson David L.,Caskey C.Thomas

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference23 articles.

1. Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome;Bell;Cell,1991

2. Random cloning and sequencing by the M13 dideoxynucleotide termination method;Bankier;Meth. Enzymol.,1987

3. The fragile X: progress towards solving the puzzle;Brown;Am. J. Hum. Genet.,1990

4. Centre d'Etude du Polymorphisme Humain (CEPH): collaborative genetic mapping of the human genome;Dausset;Genomics,1990

5. Molecular cloning and analysis of the fragile X region in man;Dietrich;Nucl. Acids Res.,1991

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