Research view

Title: Direct molecular analysis of the fragile X syndrome in a sample of Egyptian and German patients using non-radioactive PCR and Southern blot followed by chemiluminescent detection
Author: El-Aleem-AA; Bohm-I; Temtamy-S; El-Awady-M; Awadalla-M; Schmidtke-J; Stuhrmann-M
Abstract:
Molecular genetic analysis of individuals from 6 Egyptian and 33 German families with fragile X syndrome and 240 further patients with mental retardation was performed applying a completely non-radioactive system. The aim of our study was the development
Journal: HUM-GENET. 96/5 (577-584) 1995