Interpretation of the heterogeneity in the linkage relationships of DNA markers around the fragile X locus

[1]  W. Brown,et al.  Further evidence for genetic heterogeneity in the fragile X syndrome , 1987, Human Genetics.

[2]  W. Brown,et al.  Hypothesis regarding the nature of the fragile X mutation , 1987, Human Genetics.

[3]  R. Winter Population genetics implications of the premutation hypothesis for the generation of the fragile X mental retardation gene , 1987, Human Genetics.

[4]  D. Ledbetter,et al.  Implications of fragile X expression in normal males for the nature of the mutation , 1986, Nature.

[5]  M. Pembrey,et al.  Analysis of linkage relationships between genetic markers around the fragile X locus with special reference to the daughters of normal transmitting males , 1986, Human Genetics.

[6]  M. Pembrey,et al.  A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation. , 1985, American journal of medical genetics.

[7]  M. Jaye,et al.  Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male , 1983, Nature.

[8]  N. Morton,et al.  Further segregation analysis of the fragile X syndrome with special reference to transmitting males , 2004, Human Genetics.

[9]  N. Tommerup,et al.  Linkage studies of X-linked mental retardation: High frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome) , 2004, Human Genetics.

[10]  D. Ledbetter,et al.  Fragile X syndrome: a unique mutation in man. , 1986, Annual review of genetics.

[11]  D. Ledbetter,et al.  Recombination and amplification of pyrimidine-rich sequences may be responsible for initiation and progression of the Xq27 fragile site: an hypothesis. , 1986, American journal of medical genetics.

[12]  T. Rabbitts,et al.  REARRANGEMENTS OF THE C-MYC GENE IN BURKITTS-LYMPHOMA , 1984 .