Fragile site (16) (q22)
β
B. MΓΌller; W. Feichtinger; C. BonaΓ―ti-PelliΓ©; M. Schmid
π
Article
π
1992
π
Springer
π
English
β 210 KB
The rare autosomal fragile site, fra (16) (q22), is the most common of all rare autosomal fragile sites and has a heterozygote frequency of about 5%. Evidence for it was found following the segregation expected from a simple codominant trait with complete penetrance; this is in contrast to a variety