𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Prenatal diagnosis in known fragile X carriers

✍ Scribed by Maddalena, Anne ;Hicks, Belynda D. ;Spence, W. Christine ;Levinson, Gene ;Howard-Peebles, Patricia N.


Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
724 KB
Volume
51
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Prenatal diagnosis and carrier detection
✍ Von Koskull, Harriet ;NordstrΓΆm, Ann-Marie ;Salonen, Riitta ;Peltonen, Leena πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 English βš– 498 KB πŸ‘ 2 views

## Abstract Prenatal diagnosis was performed in 81 cases at risk for the fragile X syndrome. There were 12 fra (X)‐positive cases, two of which showed low expression in cultured amniotic fluid cells. FUdR and high thymidine were used for induction of fra(X) (q27.3) expression in all cases. In 21 ca

Second trimester prenatal diagnosis of t
✍ Tommerup, Niels ;Aula, Pertti ;Gustavii, BjΓΆrn ;Heiberg, Arvid ;Holmgren, GΓΆsta πŸ“‚ Article πŸ“… 1986 πŸ› John Wiley and Sons 🌐 English βš– 603 KB
Distribution of autosomal fragile sites
✍ Krawczun, Michael S. ;Jenkins, Edmund C. ;Duncan, Charlotte J. ;Stark-Houck, San πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 622 KB

We reviewed the distribution of autosomal fragile sites (FS) and spontaneous chromosome breaks or gaps (CB) at chromosome locations other than those recognized as FS from 100 amniotic fluid samples (AF), 19 chorionic villus samples (CVS), and 5 percutaneous umbilical blood samples (PUBS) referred fo