Family study of common fragile sites
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00284056.pdf
Reference9 articles.
1. Barbi G, Steinbach P, Vogel W (1984) Nonrandom distribution of methotrexate-induced aberrations on human chromosomes. Detection of further folic acid sensitive fragile sites. Hum Genet 68: 290?294
2. Berger R, Bloomfield CD, Sutherland GR (1985) Report of the committee on chromosome rearrangements in neoplasia and on fragile sites. Cytogenet Cell Genet 40:490?535
3. Eberle G, Zankl M, Zankl H (1982) The expression of fragile X chromosome in members of the same family at different times of examination. Hum Genet 61:254?255
4. Gillberg C, Wahlstrom J, Hagberg B (1984) Infantile autism and Rett's syndrome: common chromosomal denominator. Lancet II: 1094?1095
5. Herbich J, Szilvassy J, Schneld W (1985) Gene location of the PGM enzyme system and the Duffy blood groups on chromosome no. 1 by means of a new fragile site at 1p31. Hum Genet 70:178?180
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