Cited by

• Heterozygous female carriers of the marker-X-chromosome: IQ estimation and replication status of fra(X)(q).

  Paul J, Froster-Iskenius U, Moje W, Schwinger E. Paul J, et al. Hum Genet. 1984;66(4):344-6. doi: 10.1007/BF00287638. Hum Genet. 1984. PMID: 6586635
• Replication status of fragile X(q27.3) in 13 female heterozygotes.

  Tuckerman E, Webb T, Thake A. Tuckerman E, et al. J Med Genet. 1986 Oct;23(5):407-10. doi: 10.1136/jmg.23.5.407. J Med Genet. 1986. PMID: 3783617 Free PMC article.
• X-chromosome polysomy in the male. The Leuven experience 1966-1987.

  Kleczkowska A, Fryns JP, Van den Berghe H. Kleczkowska A, et al. Hum Genet. 1988 Sep;80(1):16-22. doi: 10.1007/BF00451449. Hum Genet. 1988. PMID: 3417301
• Fragile sites, chromosomal lesions, tandem repeats, and disease.

  Mirceta M, Shum N, Schmidt MHM, Pearson CE. Mirceta M, et al. Front Genet. 2022 Nov 17;13:985975. doi: 10.3389/fgene.2022.985975. eCollection 2022. Front Genet. 2022. PMID: 36468036 Free PMC article. Review.
• Further segregation analysis of the fragile X syndrome with special reference to transmitting males.

  Sherman SL, Jacobs PA, Morton NE, Froster-Iskenius U, Howard-Peebles PN, Nielsen KB, Partington MW, Sutherland GR, Turner G, Watson M. Sherman SL, et al. Hum Genet. 1985;69(4):289-99. doi: 10.1007/BF00291644. Hum Genet. 1985. PMID: 3838733