Pitfalls in the use of chromosome variants for paternity dispute cases
- 1 January 1977
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 37 (3) , 255-260
- https://doi.org/10.1007/bf00393606
Abstract
A huge ‘satellite’ (22s+) was observed in a mentally retarded and malformed girl. It consisted of constitutive heterochromatin based on the C-band technique (CBG). In neither of the parents was the variant observed. Genetic marker studies revealed that the father was, indeed, the father of the proposita (probability, 99.8%). It is emphasized that caution must be taken in the use of chromosome variants for paternity dispute cases.This publication has 14 references indexed in Scilit:
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