Rare chromosome 20 variants encountered during prenatal diagnosis
- 1 September 1986
- journal article
- research article
- Published by Wiley in Prenatal Diagnosis
- Vol. 6 (5), 363-367
- https://doi.org/10.1002/pd.1970060504
Abstract
A case with an uncommon heteromorphism in the centromeric region of chromosome 20, var (20) (cen, CBG 50), and a family with a pericentric inversion of chromosome 20, inv (20) (p11.23q11.21), are reported, both detected in amniotic fluid cell cultures. It appears that small pericentric inversions of chromosome 20 have a low risk of recombination.Keywords
This publication has 14 references indexed in Scilit:
- Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriersClinical Genetics, 2008
- Variation in the centromeric banding of chromosome 19*Clinical Genetics, 2008
- Centromere heteromorphism in chromosome 19Clinical Genetics, 2008
- Human meiosis IX. Crossing over and chiasma formation in oocytesCarlsberg Research Communications, 1985
- A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnosesPrenatal Diagnosis, 1984
- Human meiosis VI. Crossing over in human spermatocytesCarlsberg Research Communications, 1983
- Polymorphism of human chromosomes 1, 9, 16, Y: Variations, segregation and mosaicismHuman Genetics, 1982
- Variation in chromosome 19.Journal of Medical Genetics, 1979
- LBA technique in the detection of chromosome variantsHuman Genetics, 1977
- Human Q and C chromosomal variations: distribution and incidenceCytogenetic and Genome Research, 1975