An unusual karyotype in a patient with signs suggestive of Down's syndrome.
Open Access
- 1 March 1968
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 5 (1), 68-71
- https://doi.org/10.1136/jmg.5.1.68
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Cytogenetics of Down’s Syndrome (Mongolism) III. Frequency of Interchange Trisomics and Mutation Rate of Chromosome InterchangesCytogenetic and Genome Research, 1965
- Enlarged Short Arm of a Small Acrocentric Chromosome in Grandfather, Mother and Child, the Latter with Down’s SyndromeCytogenetic and Genome Research, 1964
- THE DRUMSTICKS OF POLYMORPHONUCLEAR LEUCOCYTES IN SEX-CHROMOSOME ABNORMALITIESThe Lancet, 1962
- PERICENTRIC INVERSION OF CHROMOSOME 21 A POSSIBLE FURTHER CYTOGENETIC MECHANISM IN MONGOLISMThe Lancet, 1962
- CHROMOSOME STUDIES IN DETECTION OF PARENTS WITH HIGH RISK OF SECOND CHILD WITH DOWN'S SYNDROMEThe Lancet, 1961
- Chromosome preparations of leukocytes cultured from human peripheral bloodExperimental Cell Research, 1960
- CHROMOSOMAL ABNORMALITIES IN FATHER AND MONGOL CHILDThe Lancet, 1960
- [Study of somatic chromosomes from 9 mongoloid children].1959