Exomphalos and trisomy 18 syndrome
- 1 March 1976
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 32 (2) , 221-223
- https://doi.org/10.1007/bf00291509
Abstract
A large exomphalos was found in two infants with a clinically and cytogenetically typical picture of trisomy 18 syndrome. In addition one infant was a case of male pseudohermaphroditism.This publication has 6 references indexed in Scilit:
- Chromosome examination of newborn childrenHumangenetik, 1975
- Structural abnormalities of chromosome 18. II. Two familial translocations, B-18 and 16-18, ascertained through unbalanced forms.1971
- Study of selected congenital anomalies in Pennsylvania.1967
- A Probable 17-18 Trisomy Syndrome with Phocomelia, Exomphalos, and Agenesis of HemidiaphragmArchives of Disease in Childhood, 1964