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Neonatal hyperglycemia and chromosome deletion (46,XX,Dq-)

✍ Scribed by Jaakko Leisti; Kari Raivio; Kai Krohn


Book ID
118539589
Publisher
Elsevier Science
Year
1976
Tongue
English
Weight
189 KB
Volume
88
Category
Article
ISSN
1097-6833

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Chromosome deletion [46,XX,del(20)(q11)]
✍ L. Findley; J. E. Kurnick; D. C. Peakman; A. Robinson πŸ“‚ Article πŸ“… 1979 πŸ› Springer 🌐 English βš– 310 KB

A woman in the fourth year of agnogenic myeloid metaplasia was found to have partial deletion of the long arm of chromosome 20 [46,XX,del(20)(q11)] in mitoses of presumably immature myeloid cells from unstimulated cultures of peripheral blood and bone marrow. Cytogenetic studies of peripheral blood

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✍ P. Kaiser; K. Gerhard-Ratschow; B. Zabel; E. Daume πŸ“‚ Article πŸ“… 1977 πŸ› Springer 🌐 English βš– 232 KB

A 31-year-old female patient with short stature, signs of gonadal dysgenesis, and slight Turner signs is described with a mosaic 45,XO/46,XX del (X) (qter leads to p11) determined with trypsin Giemsa-banding and C-staining. BUdR incorporation indicated the deleted X to be late replicating.