| Literature DB >> 1976593 |
B Jaume-Roig1, B Simon-Bouy, A Taillandier, J L Serre, J Antich, J Bellon, J Boué, A Boué.
Abstract
Spanish families (n = 75) with at least one affected cystic fibrosis (CF) child were typed for restriction fragment length polymorphisms (RFLPs) by the probes XV2c, KM19, and pMP6d-9. These families were also studied at the 508 mutation site by the polymerase chain reaction method. We have studied the linkage disequilibrium between these markers and the CF mutations, the probable number of independent secondary CFX (non-delta F508) mutations, and the genetic differences between Spain and Western Europe.Entities:
Mesh:
Year: 1990 PMID: 1976593 DOI: 10.1007/bf02428284
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132