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

This publication has 20 references indexed in Scilit:

• Absence of expression of the FMR-1 gene in fragile X syndrome
  Cell, 1991
• Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
  Published by Elsevier ,1991
• The CEPH consortium linkage map of human chromosome 1
  Genomics, 1991
• Isolation of Sequences that Span the Fragile X and Identification of a Fragile X-Related CpG Island
  Science, 1991
• Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis
  Nature, 1991
• Prevalence of the fragile‐X syndrome in mentally retarded boys in a Swedish county
  American Journal of Medical Genetics, 1986
• Population incidence and segregation ratios in the Martin‐Bell syndrome
  American Journal of Medical Genetics, 1986
• Further segregation analysis of the fragile X syndrome with special reference to transmitting males
  Human Genetics, 1985
• GENE AMPLIFICATION
  Annual Review of Biochemistry, 1984
• The marker (X) syndrome: a cytogenetic and genetic analysis
  Annals of Human Genetics, 1984