Mapping of an origin of DNA replication in the promoter of fragile X gene FMR1

Author:

Brylawski Bruna P.,Chastain Paul D.,Cohen Stephanie M.,Cordeiro-Stone Marila,Kaufman David G.

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Molecular Biology,Pathology and Forensic Medicine

Reference51 articles.

1. Molecular-neurobehavioral associations in females with the fragile X full mutation;Abrams;Am. J. Med. Genet.,1994

2. Role of postreplication repair in transformation of human fibroblasts to anchorage independence;Boyer;Cancer Res.,1991

3. Construction of a cosmid library of DNA replicated early in the S phase of normal human fibroblasts;Brylawski;J. Cell. Biochem.,2000

4. CTG repeats associated with human genetic disease are inherently flexible;Chastain;J. Mol. Biol.,1998

5. Anomalous rapid electrophoretic mobility of DNA containing triplet repeats associated with human disease genes;Chastain;Biochemistry,1995

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