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Fragile site long arm chromosome 16

✍ Scribed by K. Sørensen; J. Nielsen; V. Holm; J. Haahr


Publisher
Springer
Year
1979
Tongue
English
Weight
258 KB
Volume
48
Category
Article
ISSN
0340-6717

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✦ Synopsis


A fragile site at the long arms (q21) of chromosome 16 was found in two persons, each of whom became the parent of a child with a de novo structural chromosome abnormality--a balanced autosomal translocation and an autosomal deletion. The question of an increased risk of structural chromosome abnormalities in the offspring of persons with fragile site long arm 16 is discussed.


📜 SIMILAR VOLUMES


Fragile site (16) (q22)
✍ B. Müller; W. Feichtinger; C. Bonaïti-Pellié; M. Schmid 📂 Article 📅 1992 🏛 Springer 🌐 English ⚖ 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

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