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