Jaume-Roig B, Simon-Bouy B, Taillandier A, Serre J L, Antich J, Bellon J, Boué J, Boué A
Unité 73, Institut National de la Santé et de la Recherche Médicale, Paris, France.
Hum Genet. 1990 Sep;85(4):410-1. doi: 10.1007/BF02428284.
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.