Origin of the extra chromosome in trisomy 16
- 1 September 1976
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 10 (3) , 156-160
- https://doi.org/10.1111/j.1399-0004.1976.tb00028.x
Abstract
Chromosome analysis was carried out on 22 spontaneous abortuses with trisomy 16 and their parents by means of sequential Q‐ and C‐banding techniques. In seven cases, the extra chromosome No. 16 originated from a non‐disjunctional error in the first meiotic division in the mother, and in two cases from an error in the first meiotic division in the father. In two cases, non‐disjunction had occurred during the second meiotic division (one in the mother and one in the father). It seems that trisomy 16, although independent of maternal age, most frequently results from a first meiotic non‐disjunction in the mother.This publication has 6 references indexed in Scilit:
- Meiotic disjunction in T(14;15)6Ca heterozygotes and fate of chromosomally unbalanced gametes in embryonic developmentCytogenetic and Genome Research, 1975
- Trisomy in the fetal backcross progeny of male and female metacentric heterozygotes of the mouse. I.Cytogenetic and Genome Research, 1974
- Monosomy for the centromeric and juxtacentromeric region of chromosome 21Human Genetics, 1974
- ORIGIN OF THE TRISOMIC 21 CHROMOSOMEThe Lancet, 1973
- ORIGIN OF EXTRA CHROMOSOME IN TRISOMY 21The Lancet, 1973
- Origin of triploidy in human abortusesHereditas, 1972