Oberle I, et al. The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency. Proc. Natl. Acad. Sci. USA 82: 2824-2828, 1985. PubMed: 2986139
Mandel JL, et al. Genetic mapping of the human X chromosome: linkage analysis of the q26-q28 region that includes the fragile X locus and isolation of expressed sequences. Cold Spring Harbor Symp. Quant. Biol. 51: 195-203, 1986. PubMed: 3472716
Oberle I, et al. Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27. Hum. Genet. 77: 60-65, 1987. PubMed: 3502701
Vincent A, et al. The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus. Genomics 5: 797-801, 1989. PubMed: 2574147
Feil R, et al. Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, DXS134): analysis of a cosmid clone and a yeast artificial chromosome. Am. J. Hum. Genet. 46: 720-728, 1990. PubMed: 1969226
Barjon P, Schwartz C. New TaqI RFLPs at the DXS52 (St14) locus in the black population. Nucleic Acids Res. 17: 2149, 1989. PubMed: 2564665
Suthers GK, et al. Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines. Am. J. Hum. Genet. 47: 187-195, 1990. PubMed: 2378346
Jean Louis Mandel, personal communication
|