The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1990.tb03498.x/fullpdf
Reference23 articles.
1. Report of the committee on chromosome rearrangements in neoplasia and on fragile sites. (HGM8);Berger;Cytogenet. Cell Genet.,1985
2. High resolution banding and the locus of the Xq fragile site;Brookwell;Hum. Genet.,1983
3. Clinical implications and classification of the constitutive fragile sites;Daniel;Am. J. Med. Genet.,1986
4. A comparative mapping study of fragile sites in the human and murine genomes;Djalali;Hum. Genet.,1987
5. Low frequencies of apparently fragile X chromosomes in normal control cultures: a possible explanation;Jenkins;Exp. Cell Biol.,1986a
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