CHROMOSOME STUDIES IN DETECTION OF PARENTS WITH HIGH RISK OF SECOND CHILD WITH DOWN'S SYNDROME
- 7 October 1961
- journal article
- Published by Elsevier in The Lancet
- Vol. 278 (7206), 788-791
- https://doi.org/10.1016/s0140-6736(61)91086-8
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- RISK OF PARENTS WHO HAVE HAD ONE CHILD WITH DOWN'S SYNDROME (MONGOLISM) HAVING ANOTHER CHILD SIMILARLY AFFECTEDThe Lancet, 1961
- 21-TRISOMY/NORMAL MOSAICISM: in an Intelligent Child with some Mongoloid CharactersThe Lancet, 1961
- CHROMOSOME TRANSLOCATION AS A CAUSE OF FAMILIAL MONGOLISMThe Lancet, 1960
- Chromosome preparations of leukocytes cultured from human peripheral bloodExperimental Cell Research, 1960
- CHROMOSOMAL ABNORMALITIES IN FATHER AND MONGOL CHILDThe Lancet, 1960