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Prenatal cytogenetic diagnosis of the fragile X syndrome in amniotic fluid: Calculation of accuracy

✍ Scribed by Shapiro, Lawrence R. ;Wilmot, Patrick L. ;Fisch, Gene S.


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
233 KB
Volume
43
Category
Article
ISSN
0148-7299

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Prenatal cytogenetic diagnosis of the fr
✍ Shapiro, Lawrence R. ;Wilmot, Patrick L. ;Andree, Lynn E. πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 English βš– 217 KB πŸ‘ 2 views

## Abstract We have had experience with over 300 amniotic fluid specimens for prenatal diagnosis for the fragile X chromosome [fra(X)], and the flask method of tissue culture has been routinely utilized requiring extended tissue culture periods of 3–4 weeks. The use of the in situ clonal method of

Prenatal diagnosis of fragile X syndrome
✍ Murphy, Patricia D. ;Wilmot, Patrick L. ;Shapiro, Lawrence R. πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 English βš– 366 KB πŸ‘ 1 views

## Abstract Since 1985, we have provided coordinated DNA‐based and cytogenetic prenatal analysis for couples at risk for offspring afflicted with the fragile X [fra(X)] syndrome. To date, 40 pregnancies have been studied (22 males, 18 females). There were 5 males and 3 females identified to be at h