PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS WHERE SINGLE AFFECTED CHILD HAS DIED: GUTHRIE SPOTS AND MICROVILLAR ENZYME TESTING
- 5 November 1988
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 332 (8619) , 1085
- https://doi.org/10.1016/s0140-6736(88)90110-9
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- GUTHRIE SPOTS FOR DNA-BASED CARRIER TESTING IN CYSTIC FIBROSISThe Lancet, 1988
- Use of linkage disequilibrium data in prenatal diagnosis of cystic fibrosisHuman Genetics, 1988
- GUTHRIE CARDS FOR DETECTION OF POINT MUTATIONS IN PHENYLKETONURIAThe Lancet, 1988
- SAME-DAY, FIRST-TRIMESTER ANTENATAL DIAGNOSIS FOR CYSTIC FIBROSIS BY GENE AMPLIFICATIONThe Lancet, 1988
- PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS BY DNA AMPLIFICATION FOR DETECTION OF KM-19 POLYMORPHISMThe Lancet, 1988
- Prenatal diagnosis of cystic fibrosis by microvillar enzyme assay on a sequence of 258 pregnanciesHuman Genetics, 1988