18q- syndrome in mother and daughter
- 1 September 1979
- journal article
- research article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 130 (3) , 189-192
- https://doi.org/10.1007/bf00455265
Abstract
The 18q- syndrome is described in a mother and her daughter. In both of them an identical, apparently balanced 18q-/14p+ translocation was found (Karyotype: 46,XX,t(14;18)(p11;q21)), suggesting that chromosomal material was lost in the process of translocation. The segment deleted and responsible for the 18q- phenotype must be located in or near band 18q21, in which the break is assumed to have occurred.This publication has 4 references indexed in Scilit:
- A cytogenetic survey of an institution for the mentally retarded: I. Chromosome abnormalitiesClinical Genetics, 2008
- [18 q deletion in mother and daughter (author's transl)].1976
- Familial occurrence of 18q-Human Genetics, 1970
- [Partial deletion of the long arm of chromosome 18. Individualization of a new morbid state].1966