Familial Down's syndrome A cytogenetical and genealogical study of twenty-two families
- 1 November 1966
- journal article
- research article
- Published by Wiley in Annals of Human Genetics
- Vol. 30 (2), 125-146
- https://doi.org/10.1111/j.1469-1809.1966.tb00013.x
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- CHROMOSOME STUDIES ON RANDOMLY CHOSEN MEN AND WOMENThe Lancet, 1965
- Cytogenetics of Down’s Syndrome (Mongolism) I. Data on a Consecutive Series of Patients Referred for Genetic Counselling and DiagnosisCytogenetic and Genome Research, 1965
- Cytogenetics of Down’s Syndrome (Mongolism) II. The Frequency of Interchange Trisomy in Patients Born at a Maternal Age of less than 30 YearsCytogenetic and Genome Research, 1965
- TWO UNUSUAL CASES OF FAMILIAL MONGOLISMCanadian Journal of Genetics and Cytology, 1964
- A MICROMETHOD FOR CHROMOSOME ANALYSIS ON PERIPHERAL BLOOD-CULTURESThe Lancet, 1962
- CHROMOSOME STUDIES IN DETECTION OF PARENTS WITH HIGH RISK OF SECOND CHILD WITH DOWN'S SYNDROMEThe Lancet, 1961
- MONGOLISM*British Medical Bulletin, 1961
- CHROMOSOME TRANSLOCATION AS A CAUSE OF FAMILIAL MONGOLISMThe Lancet, 1960
- Chromosome preparations of leukocytes cultured from human peripheral bloodExperimental Cell Research, 1960
- CHROMOSOMAL TRANSLOCATIONS IN MONGOLISM AND IN NORMAL RELATIVESThe Lancet, 1960