OVARIAN DYSGENESIS AND CHROMOSOME-ABNORMALITIES
- 1 January 1977
- journal article
- research article
- Vol. 50 (1) , 13-20
Abstract
The association of ovarian hypoplasia with trisomy 18 in 6 infants and trisomy 13 in 5 infants and 1 fetus is reported. Three infants also had thymic hypoplasia. The possible etiology of ovarian dysgenesis is discussed in relation to a variety of clinical and experimental associations.This publication has 8 references indexed in Scilit:
- Trisomy 13 (D1) syndrome: Studies on parentalage, sex ratio, and survivalThe Journal of Pediatrics, 1968
- Absence of Thymus in a Mouse MutantNature, 1968
- Oogenesis in the mouseExperimental Cell Research, 1967
- ‘Nude’, a new hairless gene with pleiotropic effects in the mouseGenetics Research, 1966
- The anatomy and histology of XO human embryos and fetusesThe Anatomical Record, 1966
- ATAXIA-TELANGIECTASIA1964
- A quantitative and cytological study of germ cells in human ovariesProceedings of the Royal Society of London. B. Biological Sciences, 1963
- Embryological phases of mammalian gametogenesisJournal of Cellular and Comparative Physiology, 1960