POLYMORPHIC DNA MARKERS IN PRENATAL DIAGNOSIS OF FRAGILE X SYNDROME
- 13 April 1985
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 325 (8433), 871
- https://doi.org/10.1016/s0140-6736(85)92228-7
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.Proceedings of the National Academy of Sciences, 1985
- Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphismsNucleic Acids Research, 1984
- The marker (X) syndrome: a cytogenetic and genetic analysisAnnals of Human Genetics, 1984
- Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).Proceedings of the National Academy of Sciences, 1984
- Experience with prenatal fragile X detectionAmerican Journal of Medical Genetics, 1984
- PRENATAL DIAGNOSIS OF MARTIN-BELL SYNDROME ASSOCIATED WITH FRAGILE SITE AT Xq27-28The Lancet, 1981
- FEASIBILITY OF FRAGILE X CHROMOSOME PRENATAL DIAGNOSIS DEMONSTRATEDThe Lancet, 1981