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Partial deletion of the X chromosome in gonadal dysgenesis 46,X,del(X)(p22) identified by BUdR treatment

✍ Scribed by P. Petrinelli; A. Antonelli; P. Gabellini; F. Gigliani; L. Marcucci; B. Nicoletti


Publisher
Springer
Year
1978
Tongue
English
Weight
336 KB
Volume
45
Category
Article
ISSN
0340-6717

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✦ Synopsis


In this report we describe a deletion of the short arm of the X chromosome in a 16-year-old female with gonadal dysgenesis. The breakpoint was localized by BUdR treatment and acridine orange staining in region 2, band 2. Of the examined cells, 3% showed an early replication of the deleted X chromosome.


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