Population screening for fragile-X syndrome
β Scribed by Bonthron, David; Strain, Lisa; Bundey, Sarah; Norman, Elizabeth; Howard-Peebles, PatriciaN.; Maddalena, Anne; Black, SusanH.; Schulman, JosephD.
- Book ID
- 123190582
- Publisher
- The Lancet
- Year
- 1993
- Tongue
- English
- Weight
- 426 KB
- Volume
- 341
- Category
- Article
- ISSN
- 0140-6736
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract Molecular diagnosis of Fragile X Syndrome (FXS) is carried out by PCR or Southern blot analysis on DNA isolated from leukocytes. These DNA analyses are time consuming and expensive, making it impractical for mass screening programs. We have recently standardized and tested the diagnosti
## Abstract Population carrier screening for fragile X syndrome can provide women with information about their risk of having a child with fragile X syndrome and their risk of fragile Xβassociated primary ovarian insufficiency and fragile Xβassociated tremor ataxia syndrome. Few studies have explor
## Abstract Newborn screening for fragile X syndrome (FXS) is technically possible, and in the relatively near future accurate and inexpensive screening technologies are likely to be available. When that happens, will America's public health system adopt newborn screening for fragile X syndrome? Th