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
β¦ LIBER β¦
The fragile site (16)(q22)
β Scribed by M. Schmid; W. Feichtinger; T. Haaf
- Publisher
- Springer
- Year
- 1987
- Tongue
- English
- Weight
- 591 KB
- Volume
- 76
- Category
- Article
- ISSN
- 0340-6717
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