A female infant with monosomy 21
- 1 January 1976
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 31 (3) , 351-353
- https://doi.org/10.1007/bf00270866
Abstract
A female infant with total monosomy 21 identified by Q banding is described. The main clinical features were hypertonia, prominent occiput, hypertelorism, antimongoloid slant of the eyes, broad nose, “antimongoloid” character of dermatoglyphics. Both parents are phenotypically as well as karyotypically normal.Keywords
This publication has 3 references indexed in Scilit:
- A male infant with monosomy 21Human Genetics, 1975
- Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes.1973
- The G deletion syndromesThe Journal of Pediatrics, 1970