Multilocus analysis of the fragile X syndrome

W. T. Brown, A. Gross, C. Chan, E. C. Jenkins, J. L. Mandel, I. Oberlé, B. Arveiler, G. Novelli, S. Thibodeau, R. Hagerman, K. Summers, G. Turner, B. N. White, L. Mulligan, C. Forster-Gibson, J. J.A. Holden, B. Zoll, M. Krawczak, P. Goonewardena, K. H. GustavsonU. Pettersson, G. Holmgren, C. Schwartz, P. N. Howard-Peebles, P. Murphy, W. R. Breg, H. Veenema, N. J. Carpenter

Research output: Contribution to journalArticlepeer-review

24 Scopus citations


A multilocus analysis of the fragile X (fra(X)) syndrome was conducted with 147 families. Two proximal loci, DXS51 and F9, and two distal loci, DXS52 and DXS15, were studied. Overall, the best multipoint distances were found to be DXS51-F9, 6.9%, F9-fra(X), 22.4%; fra(X)-DXS52, 12.7%; DXS52-DXS15, 2.2%. These distances can be used for multipoint mapping of new probes, carrier testing and counseling of fra(X) families. Consistent with several previous studies, the families as a whole showed genetic heterogeneity for linkage between F9 and fra(X).

Original languageEnglish (US)
Pages (from-to)201-205
Number of pages5
JournalHuman genetics
Issue number3
StatePublished - Mar 1988

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)


Dive into the research topics of 'Multilocus analysis of the fragile X syndrome'. Together they form a unique fingerprint.

Cite this