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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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Fra(X)(q27.2), the common fragile site,
✍ Jenkins, Edmund C. ;Genovese, Marilyn J. ;Duncan, Charlotte J. ;Gu, Hong ;Stark- 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 382 KB 👁 2 views

## 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