Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission karyotype: 46,XX,-13,+t(13;13)(p11;q11)/46,XX,del(13)(p11)
- 1 January 1979
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 46 (2) , 237-241
- https://doi.org/10.1007/bf00291927
Abstract
A severely retarded child with multiple malformations was found to present a mosaic karyotype 46,XX,-13,+t(13;13)(p11;q11)/46,XX,del (13)(p11), which probably originated as the result of a de novo 13/13 translocation in a parental gamete, followed by postzygotic fission of the translocation chromosomse.This publication has 8 references indexed in Scilit:
- Induced Robertsonian fusions and tandem translocations in mammalian cell culturesCytogenetic and Genome Research, 1978
- Structure and inheritance of some heterozygous Robertsonian translocation in man.Journal of Medical Genetics, 1976
- Trisomy 13 Mosaic Presenting as Cleft Lip and PalateHuman Heredity, 1975
- Cleft lip and cleft palate in D trisomy.1975
- Reciprocal translocation versus centric fusion between two No. 13 chromosomesCytogenetic and Genome Research, 1973
- [Mosaic trisomy 13 with isochromosome: 46, XX-46, XX, 13-, 13 q:].1972
- Trisomy D1 Syndrome With DqDq Tandem TranslocationArchives of Pediatrics & Adolescent Medicine, 1971
- Trisomy 13 (D1) syndrome: Studies on parentalage, sex ratio, and survivalThe Journal of Pediatrics, 1968