| Literature DB >> 65472 |
R L Neu, C C Ortega, G A Barg, W Pinto, L I Gardner, W M Howell, T E Denton.
Abstract
A male infant with a partial trisomy 18 and a 46,XY, --21, t(18;21)(18qter replaced by 18q12::21 p13 replaced by 21 qter) chromosome complement is described. The translocation chromosome is of special interest because it includes the satellites of chromosome 21. This was shown by differential satellite staining with the ammoniacal-silver technique.Entities:
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Year: 1976 PMID: 65472 PMCID: PMC1013484 DOI: 10.1136/jmg.13.6.520
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318