Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18.
- 1 December 1976
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 13 (6) , 520-522
- https://doi.org/10.1136/jmg.13.6.520
Abstract
A male infant with a partial trisomy 18 and a 46,XY,-21,t(18;21)(18qter.fwdarw.18q12::21p13.fwdarw.21qter) 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.This publication has 16 references indexed in Scilit:
- Differential staining of the satellite regions of human acrocentric chromosomesCellular and Molecular Life Sciences, 1975
- SATELLITE STAINING OF HUMAN CHROMOSOMESThe Lancet, 1974
- Differential Staining of Nucleolus Organisers in Mammalian ChromosomesNature, 1973
- Ribosomal DNA Connectives between Human Acrocentric ChromosomesNature, 1973
- The mechanism of C- and G-banding of chromosomesExperimental Cell Research, 1973
- Gene deletion and duplication effects on phenotype and gamma globulin levels.Journal of Medical Genetics, 1971
- Trisomy 16-18 in the Bantu.1967
- A NEW TRISOMY-TRANSLOCATION CHROMOSOME (LONG-ARM E/E)The Lancet, 1963
- TRISOMY-18 SYNDROME DUE TO DE-NOVO TRANSLOCATIONThe Lancet, 1963
- The E syndrome (trisomy 17-18) resulting from a maternal chromosomal translocation.1962