The trisomy 18 syndrome with an E/G translocation
- 1 January 1976
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 31 (3), 347-349
- https://doi.org/10.1007/bf00270865
Abstract
An infant with a typical Edwards syndrome and a modal chromosome number of 46 is reported. In all cells analyzed one chromosome G was missing and an additional chromosome similar to a pair No. 16 was present. The phenotype of the child indicates that the extra element is a translocation between G and 18 chromosomes as in one case described previously.This publication has 6 references indexed in Scilit:
- Trisomy 18 with an E-G translocation (46,XY,21-t(21q18q)+). Identification of the component chromosomes by several laboratory techniques.1972
- Structural abnormalities of chromosome 18. II. Two familial translocations, B-18 and 16-18, ascertained through unbalanced forms.1971
- A NEW TRISOMY-TRANSLOCATION CHROMOSOME (LONG-ARM E/E)The Lancet, 1963
- [Partial trisomy 18 caused by insertion or translocation 4/18].1963
- TRISOMY-18 SYNDROME DUE TO DE-NOVO TRANSLOCATIONThe Lancet, 1963
- The E syndrome (trisomy 17-18) resulting from a maternal chromosomal translocation.1962