FIRST TRIMESTER PRENATAL DIAGNOSIS OF A MALE FETUS WITH FRAGILE X
Open Access
- 1 April 1985
- journal article
- Published by Elsevier in The Lancet
- Vol. 325 (8433), 870
- https://doi.org/10.1016/s0140-6736(85)92227-5
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphismsNucleic Acids Research, 1984
- Efficient direct chromosome analyses and enzyme determinations from chorionic villi samples in the first trimester of pregnancyHuman Genetics, 1983
- Human amniotic fluid cells grown in a hormone-supplemented medium: suitability for prenatal diagnosis.Proceedings of the National Academy of Sciences, 1982
- A simple method to demonstrate the fragile X chromosome in fibroblastsHuman Genetics, 1981
- Expression in lymphocyte and fibroblast culture of the fragile X chromosome: A new technical approachHuman Genetics, 1981
- Marker X chromosome induction in fibroblasts by FUdRAmerican Journal of Medical Genetics, 1981