Collaborative prospective study of the fragile X syndrome: One-year progress report
✍ Scribed by Sherman, S. L. ;Barbi, G. ;Brøndum-Nielsen, K. ;Brown, W. T. ;Carpenter, N. J. ;Chudley, A. E. ;Ferraz, O. P. ;Ferreira, P. ;Gustavson, K-H. ;Halliday, J. ;Hockey, A. ;Howard-Peebles, P. N. ;Jenkins, E. ;Kennerknecht, I. ;Kähkönen, M. ;Ladaïque, P. ;Leisti, J. ;Maddalena, A. ;Mazurczak, T. ;Mattei, J-F. ;Mattina, T. ;McKinley, M. J. ;Murphy, P. ;Pellissier, M. C. ;Purvis-Smith, S. ;Robinson, H. ;Scapagnini, U. ;Schaap, T. ;Shapiro, L. R. ;Smits, A. P. T. ;Steinbach, P. ;Turner, G. ;Uchida, I. A. ;Van Oost, B. A. ;Voelckel, M-A. ;Weaver, D. D. ;Webb, T.
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 422 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0148-7299
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## Abstract Cell cultures from 760 whole blood, amniotic fluid, chorionic villus sample, and peripheral umbilical blood sample specimens were exposed to multiple fra(X)(q27.3) induction systems (none had aphidicolin). Fifty‐three exhibited the rare fragile site, fra(X)(q27.3) or FRAXA, none of whic