Down’s Syndrome Associated with a Familial (21q—;22q+) Translocation
- 1 January 1967
- journal article
- research article
- Published by S. Karger AG in Cytogenetic and Genome Research
- Vol. 6 (5), 321-330
- https://doi.org/10.1159/000154936
Abstract
A family possessing two mongoloid sibs and three balanced heterozygous carriers for a non-centric translocation between the long arm of a No. 21 and long arm of a No. 22 chromosome, yielding a medium-size acrocentric marker, is presented. In addition, the mother of the propositi, her brother and mother possessed a small, satellited centric fragment which is presumed to be the reciprocal element of the translocation.This publication has 4 references indexed in Scilit:
- Maternal transmission of a 21/1 translocation associated with Down's syndromeThe Journal of Pediatrics, 1966
- A New Cytogenetic Variant of Translocation Down’s SyndromeCytogenetic and Genome Research, 1966
- Familial Down's syndrome with undetected translocationThe Journal of Pediatrics, 1965
- Chromosome preparations of leukocytes cultured from human peripheral bloodExperimental Cell Research, 1960